Target Gene/Pathway Pathway / Gene

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No.	KEGG PATHWAY On map, Yellow: Drug target, Red: All disease-related	KEGG GENES	KEGG DRUG	DrugBank	Disease ID
1	Adrenergic signaling in cardiomyocytes 💬	[4] P38, P38, P38, P38 💬 Adrenergic signaling in cardiomyocytes × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 1. Adrenergic signaling in cardiomyocytes × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
2	Adrenergic signaling in cardiomyocytes 💬	[4] P38, P38, P38, P38 💬 Adrenergic signaling in cardiomyocytes × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Adrenergic signaling in cardiomyocytes × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 2. Adrenergic signaling in cardiomyocytes × Disease ID Name  8  Huntington disease;Huntington chorea;
3	AGE-RAGE signaling pathway in diabetic complications 💬	[4] P38, P38, P38, P38 💬 AGE-RAGE signaling pathway in diabetic complications × Name Full Name P38 P38 P38 P38	Losmapimod 💬 AGE-RAGE signaling pathway in diabetic complications × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 3. AGE-RAGE signaling pathway in diabetic complications × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
4	AGE-RAGE signaling pathway in diabetic complications 💬	[4] P38, P38, P38, P38 💬 AGE-RAGE signaling pathway in diabetic complications × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 AGE-RAGE signaling pathway in diabetic complications × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 4. AGE-RAGE signaling pathway in diabetic complications × Disease ID Name  8  Huntington disease;Huntington chorea;
5	Alcoholic liver disease 💬	[4] P38, P38, P38, P38 💬 Alcoholic liver disease × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Alcoholic liver disease × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 5. Alcoholic liver disease × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
6	Alcoholic liver disease 💬	[4] P38, P38, P38, P38 💬 Alcoholic liver disease × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Alcoholic liver disease × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 6. Alcoholic liver disease × Disease ID Name  8  Huntington disease;Huntington chorea;
7	Amyotrophic lateral sclerosis 💬	[4] P38, P38, P38, P38 💬 Amyotrophic lateral sclerosis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Amyotrophic lateral sclerosis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 7. Amyotrophic lateral sclerosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
8	Amyotrophic lateral sclerosis 💬	[4] P38, P38, P38, P38 💬 Amyotrophic lateral sclerosis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Amyotrophic lateral sclerosis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 8. Amyotrophic lateral sclerosis × Disease ID Name  8  Huntington disease;Huntington chorea;
9	C-type lectin receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 C-type lectin receptor signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 C-type lectin receptor signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 8. Amyotrophic lateral sclerosis × Disease ID Name  8  Huntington disease;Huntington chorea;
10	C-type lectin receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 C-type lectin receptor signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 C-type lectin receptor signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 10. C-type lectin receptor signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
11	Cellular senescence 💬	[4] P38, P38, P38, P38 💬 Cellular senescence × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Cellular senescence × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 10. C-type lectin receptor signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
12	Cellular senescence 💬	[4] P38, P38, P38, P38 💬 Cellular senescence × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Cellular senescence × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 12. Cellular senescence × Disease ID Name  8  Huntington disease;Huntington chorea;
13	Chagas disease 💬	[4] P38, P38, P38, P38 💬 Chagas disease × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Chagas disease × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 12. Cellular senescence × Disease ID Name  8  Huntington disease;Huntington chorea;
14	Chagas disease 💬	[4] P38, P38, P38, P38 💬 Chagas disease × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Chagas disease × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 14. Chagas disease × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
15	Chemical carcinogenesis - reactive oxygen species 💬	[4] P38, P38, P38, P38 💬 Chemical carcinogenesis - reactive oxygen species × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Chemical carcinogenesis - reactive oxygen species × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 14. Chagas disease × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
16	Chemical carcinogenesis - reactive oxygen species 💬	[4] P38, P38, P38, P38 💬 Chemical carcinogenesis - reactive oxygen species × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Chemical carcinogenesis - reactive oxygen species × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 16. Chemical carcinogenesis - reactive oxygen species × Disease ID Name  8  Huntington disease;Huntington chorea;
17	Coronavirus disease - COVID-19 💬	[4] P38, P38, P38, P38 💬 Coronavirus disease - COVID-19 × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Coronavirus disease - COVID-19 × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 17. Coronavirus disease - COVID-19 × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
18	Coronavirus disease - COVID-19 💬	[4] P38, P38, P38, P38 💬 Coronavirus disease - COVID-19 × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Coronavirus disease - COVID-19 × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 18. Coronavirus disease - COVID-19 × Disease ID Name  8  Huntington disease;Huntington chorea;
19	Diabetic cardiomyopathy 💬	[4] P38, P38, P38, P38 💬 Diabetic cardiomyopathy × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Diabetic cardiomyopathy × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 18. Coronavirus disease - COVID-19 × Disease ID Name  8  Huntington disease;Huntington chorea;
20	Diabetic cardiomyopathy 💬	[4] P38, P38, P38, P38 💬 Diabetic cardiomyopathy × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Diabetic cardiomyopathy × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 20. Diabetic cardiomyopathy × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
21	Dopaminergic synapse 💬	[4] P38, P38, P38, P38 💬 Dopaminergic synapse × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Dopaminergic synapse × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 20. Diabetic cardiomyopathy × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
22	Dopaminergic synapse 💬	[4] P38, P38, P38, P38 💬 Dopaminergic synapse × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Dopaminergic synapse × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 22. Dopaminergic synapse × Disease ID Name  8  Huntington disease;Huntington chorea;
23	Efferocytosis 💬	[4] P38, P38, P38, P38 💬 Efferocytosis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Efferocytosis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 22. Dopaminergic synapse × Disease ID Name  8  Huntington disease;Huntington chorea;
24	Efferocytosis 💬	[4] P38, P38, P38, P38 💬 Efferocytosis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Efferocytosis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 24. Efferocytosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
25	Epithelial cell signaling in Helicobacter pylori infection 💬	[4] P38, P38, P38, P38 💬 Epithelial cell signaling in Helicobacter pylori infection × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Epithelial cell signaling in Helicobacter pylori infection × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 24. Efferocytosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
26	Epithelial cell signaling in Helicobacter pylori infection 💬	[4] P38, P38, P38, P38 💬 Epithelial cell signaling in Helicobacter pylori infection × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Epithelial cell signaling in Helicobacter pylori infection × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 26. Epithelial cell signaling in Helicobacter pylori infection × Disease ID Name  8  Huntington disease;Huntington chorea;
27	Epstein-Barr virus infection 💬	[4] P38, P38, P38, P38 💬 Epstein-Barr virus infection × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Epstein-Barr virus infection × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 27. Epstein-Barr virus infection × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
28	Epstein-Barr virus infection 💬	[4] P38, P38, P38, P38 💬 Epstein-Barr virus infection × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Epstein-Barr virus infection × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 28. Epstein-Barr virus infection × Disease ID Name  8  Huntington disease;Huntington chorea;
29	Fc epsilon RI signaling pathway 💬	[4] P38, P38, P38, P38 💬 Fc epsilon RI signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Fc epsilon RI signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 29. Fc epsilon RI signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
30	Fc epsilon RI signaling pathway 💬	[4] P38, P38, P38, P38 💬 Fc epsilon RI signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Fc epsilon RI signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 30. Fc epsilon RI signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
31	Fluid shear stress and atherosclerosis 💬	[4] P38, P38, P38, P38 💬 Fluid shear stress and atherosclerosis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Fluid shear stress and atherosclerosis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 30. Fc epsilon RI signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
32	Fluid shear stress and atherosclerosis 💬	[4] P38, P38, P38, P38 💬 Fluid shear stress and atherosclerosis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Fluid shear stress and atherosclerosis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 32. Fluid shear stress and atherosclerosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
33	FoxO signaling pathway 💬	[4] P38, P38, P38, P38 💬 Fluid shear stress and atherosclerosis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 FoxO signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 32. Fluid shear stress and atherosclerosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
34	FoxO signaling pathway 💬	[4] P38, P38, P38, P38 💬 Fluid shear stress and atherosclerosis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 FoxO signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 34. FoxO signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
35	GnRH signaling pathway 💬	[4] P38, P38, P38, P38 💬 GnRH signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 GnRH signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 35. GnRH signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
36	GnRH signaling pathway 💬	[4] P38, P38, P38, P38 💬 GnRH signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 GnRH signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 36. GnRH signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
37	Growth hormone synthesis, secretion and action 💬	[4] P38, P38, P38, P38 💬 Growth hormone synthesis, secretion and action × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Growth hormone synthesis, secretion and action × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 37. Growth hormone synthesis, secretion and action × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
38	Growth hormone synthesis, secretion and action 💬	[4] P38, P38, P38, P38 💬 Growth hormone synthesis, secretion and action × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Growth hormone synthesis, secretion and action × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 38. Growth hormone synthesis, secretion and action × Disease ID Name  8  Huntington disease;Huntington chorea;
39	Hepatitis B 💬	[4] P38, P38, P38, P38 💬 Hepatitis B × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Hepatitis B × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 39. Hepatitis B × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
40	Hepatitis B 💬	[4] P38, P38, P38, P38 💬 Hepatitis B × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Hepatitis B × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 40. Hepatitis B × Disease ID Name  8  Huntington disease;Huntington chorea;
41	Human cytomegalovirus infection 💬	[4] P38, P38, P38, P38 💬 Human cytomegalovirus infection × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Human cytomegalovirus infection × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 41. Human cytomegalovirus infection × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
42	Human cytomegalovirus infection 💬	[4] P38, P38, P38, P38 💬 Human cytomegalovirus infection × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Human cytomegalovirus infection × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 42. Human cytomegalovirus infection × Disease ID Name  8  Huntington disease;Huntington chorea;
43	Human immunodeficiency virus 1 infection 💬	[4] P38, P38, P38, P38 💬 Human immunodeficiency virus 1 infection × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Human immunodeficiency virus 1 infection × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 43. Human immunodeficiency virus 1 infection × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
44	Human immunodeficiency virus 1 infection 💬	[4] P38, P38, P38, P38 💬 Human immunodeficiency virus 1 infection × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Human immunodeficiency virus 1 infection × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 44. Human immunodeficiency virus 1 infection × Disease ID Name  8  Huntington disease;Huntington chorea;
45	IL-17 signaling pathway 💬	[4] P38, P38, P38, P38 💬 IL-17 signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 IL-17 signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 45. IL-17 signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
46	IL-17 signaling pathway 💬	[4] P38, P38, P38, P38 💬 IL-17 signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 IL-17 signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 46. IL-17 signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
47	Inflammatory mediator regulation of TRP channels 💬	[4] P38, P38, P38, P38 💬 Inflammatory mediator regulation of TRP channels × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Inflammatory mediator regulation of TRP channels × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 47. Inflammatory mediator regulation of TRP channels × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
48	Inflammatory mediator regulation of TRP channels 💬	[4] P38, P38, P38, P38 💬 Inflammatory mediator regulation of TRP channels × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Inflammatory mediator regulation of TRP channels × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 48. Inflammatory mediator regulation of TRP channels × Disease ID Name  8  Huntington disease;Huntington chorea;
49	Kaposi sarcoma-associated herpesvirus infection 💬	[4] P38, P38, P38, P38 💬 Kaposi sarcoma-associated herpesvirus infection × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Kaposi sarcoma-associated herpesvirus infection × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 49. Kaposi sarcoma-associated herpesvirus infection × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
50	Kaposi sarcoma-associated herpesvirus infection 💬	[4] P38, P38, P38, P38 💬 Kaposi sarcoma-associated herpesvirus infection × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Kaposi sarcoma-associated herpesvirus infection × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 50. Kaposi sarcoma-associated herpesvirus infection × Disease ID Name  8  Huntington disease;Huntington chorea;
51	Leishmaniasis 💬	[4] P38, P38, P38, P38 💬 Leishmaniasis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Leishmaniasis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 51. Leishmaniasis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
52	Leishmaniasis 💬	[4] P38, P38, P38, P38 💬 Leishmaniasis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Leishmaniasis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 52. Leishmaniasis × Disease ID Name  8  Huntington disease;Huntington chorea;
53	Leukocyte transendothelial migration 💬	[4] P38, P38, P38, P38 💬 Leukocyte transendothelial migration × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Leukocyte transendothelial migration × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 52. Leishmaniasis × Disease ID Name  8  Huntington disease;Huntington chorea;
54	Leukocyte transendothelial migration 💬	[4] P38, P38, P38, P38 💬 Leukocyte transendothelial migration × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Leukocyte transendothelial migration × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 54. Leukocyte transendothelial migration × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
55	Lipid and atherosclerosis 💬	[4] P38, P38, P38, P38 💬 Lipid and atherosclerosis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Lipid and atherosclerosis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 55. Lipid and atherosclerosis × Disease ID Name  8  Huntington disease;Huntington chorea;
56	Lipid and atherosclerosis 💬	[4] P38, P38, P38, P38 💬 Lipid and atherosclerosis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Lipid and atherosclerosis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 56. Lipid and atherosclerosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
57	MAPK signaling pathway 💬	[4] P38, P38, P38, P38 💬 MAPK signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 MAPK signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 56. Lipid and atherosclerosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
58	MAPK signaling pathway 💬	[4] P38, P38, P38, P38 💬 MAPK signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 MAPK signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 58. MAPK signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
59	Neurotrophin signaling pathway 💬	[4] P38, P38, P38, P38 💬 Neurotrophin signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Neurotrophin signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 59. Neurotrophin signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
60	Neurotrophin signaling pathway 💬	[4] P38, P38, P38, P38 💬 Neurotrophin signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Neurotrophin signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 60. Neurotrophin signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
61	Neutrophil extracellular trap formation 💬	[4] P38, P38, P38, P38 💬 Neurotrophin signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Neutrophil extracellular trap formation × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 60. Neurotrophin signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
62	Neutrophil extracellular trap formation 💬	[4] P38, P38, P38, P38 💬 Neutrophil extracellular trap formation × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Neutrophil extracellular trap formation × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 62. Neutrophil extracellular trap formation × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
63	NOD-like receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 NOD-like receptor signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 NOD-like receptor signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 62. Neutrophil extracellular trap formation × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
64	NOD-like receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 NOD-like receptor signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 NOD-like receptor signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 64. NOD-like receptor signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
65	Non-alcoholic fatty liver disease 💬	[4] P38, P38, P38, P38 💬 Non-alcoholic fatty liver disease × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Non-alcoholic fatty liver disease × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 64. NOD-like receptor signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
66	Non-alcoholic fatty liver disease 💬	[4] P38, P38, P38, P38 💬 Non-alcoholic fatty liver disease × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Non-alcoholic fatty liver disease × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 66. Non-alcoholic fatty liver disease × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
67	Oocyte meiosis 💬	[4] P38, P38, P38, P38 💬 Oocyte meiosis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Oocyte meiosis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 67. Oocyte meiosis × Disease ID Name  8  Huntington disease;Huntington chorea;
68	Oocyte meiosis 💬	[4] P38, P38, P38, P38 💬 Oocyte meiosis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Oocyte meiosis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 68. Oocyte meiosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
69	Osteoclast differentiation 💬	[4] P38, P38, P38, P38 💬 Osteoclast differentiation × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Osteoclast differentiation × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 68. Oocyte meiosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
70	Osteoclast differentiation 💬	[4] P38, P38, P38, P38 💬 Osteoclast differentiation × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Osteoclast differentiation × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 70. Osteoclast differentiation × Disease ID Name  8  Huntington disease;Huntington chorea;
71	Pathogenic Escherichia coli infection 💬	[4] P38, P38, P38, P38 💬 Pathogenic Escherichia coli infection × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Pathogenic Escherichia coli infection × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 71. Pathogenic Escherichia coli infection × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
72	Pathogenic Escherichia coli infection 💬	[4] P38, P38, P38, P38 💬 Pathogenic Escherichia coli infection × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Pathogenic Escherichia coli infection × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 72. Pathogenic Escherichia coli infection × Disease ID Name  8  Huntington disease;Huntington chorea;
73	Pathways of neurodegeneration - multiple diseases 💬	[4] P38, P38, P38, P38 💬 Pathways of neurodegeneration - multiple diseases × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 72. Pathogenic Escherichia coli infection × Disease ID Name  8  Huntington disease;Huntington chorea;
74	Pathways of neurodegeneration - multiple diseases 💬	[4] P38, P38, P38, P38 💬 Pathways of neurodegeneration - multiple diseases × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Pathways of neurodegeneration - multiple diseases × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 74. Pathways of neurodegeneration - multiple diseases × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
75	PD-L1 expression and PD-1 checkpoint pathway in cancer 💬	[4] P38, P38, P38, P38 💬 PD-L1 expression and PD-1 checkpoint pathway in cancer × Name Full Name P38 P38 P38 P38	Losmapimod 💬 PD-L1 expression and PD-1 checkpoint pathway in cancer × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 74. Pathways of neurodegeneration - multiple diseases × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
76	PD-L1 expression and PD-1 checkpoint pathway in cancer 💬	[4] P38, P38, P38, P38 💬 PD-L1 expression and PD-1 checkpoint pathway in cancer × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 PD-L1 expression and PD-1 checkpoint pathway in cancer × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 76. PD-L1 expression and PD-1 checkpoint pathway in cancer × Disease ID Name  8  Huntington disease;Huntington chorea;
77	Pertussis 💬	[4] P38, P38, P38, P38 💬 Pertussis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Pertussis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 76. PD-L1 expression and PD-1 checkpoint pathway in cancer × Disease ID Name  8  Huntington disease;Huntington chorea;
78	Pertussis 💬	[4] P38, P38, P38, P38 💬 Pertussis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Pertussis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 78. Pertussis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
79	Platelet activation 💬	[4] P38, P38, P38, P38 💬 Platelet activation × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Platelet activation × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 78. Pertussis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
80	Platelet activation 💬	[4] P38, P38, P38, P38 💬 Platelet activation × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Platelet activation × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 80. Platelet activation × Disease ID Name  8  Huntington disease;Huntington chorea;
81	Prion disease 💬	[4] P38, P38, P38, P38 💬 Prion disease × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Prion disease × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 81. Prion disease × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
82	Prion disease 💬	[4] P38, P38, P38, P38 💬 Prion disease × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Prion disease × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 82. Prion disease × Disease ID Name  8  Huntington disease;Huntington chorea;
83	Progesterone-mediated oocyte maturation 💬	[4] P38, P38, P38, P38 💬 Progesterone-mediated oocyte maturation × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Progesterone-mediated oocyte maturation × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 82. Prion disease × Disease ID Name  8  Huntington disease;Huntington chorea;
84	Progesterone-mediated oocyte maturation 💬	[4] P38, P38, P38, P38 💬 Progesterone-mediated oocyte maturation × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Progesterone-mediated oocyte maturation × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 84. Progesterone-mediated oocyte maturation × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
85	Prolactin signaling pathway 💬	[4] P38, P38, P38, P38 💬 Prolactin signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Prolactin signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 85. Prolactin signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
86	Prolactin signaling pathway 💬	[4] P38, P38, P38, P38 💬 Prolactin signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Prolactin signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 86. Prolactin signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
87	Proteoglycans in cancer 💬	[4] P38, P38, P38, P38 💬 Proteoglycans in cancer × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Proteoglycans in cancer × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 86. Prolactin signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
88	Proteoglycans in cancer 💬	[4] P38, P38, P38, P38 💬 Proteoglycans in cancer × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Proteoglycans in cancer × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 88. Proteoglycans in cancer × Disease ID Name  8  Huntington disease;Huntington chorea;
89	Rap1 signaling pathway 💬	[4] P38, P38, P38, P38 💬 Rap1 signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Rap1 signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 89. Rap1 signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
90	Rap1 signaling pathway 💬	[4] P38, P38, P38, P38 💬 Rap1 signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Rap1 signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 90. Rap1 signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
91	Relaxin signaling pathway 💬	[4] P38, P38, P38, P38 💬 Relaxin signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Relaxin signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 90. Rap1 signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
92	Relaxin signaling pathway 💬	[4] P38, P38, P38, P38 💬 Relaxin signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Relaxin signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 92. Relaxin signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
93	Retrograde endocannabinoid signaling 💬	[4] P38, P38, P38, P38 💬 Retrograde endocannabinoid signaling × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Retrograde endocannabinoid signaling × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 92. Relaxin signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
94	Retrograde endocannabinoid signaling 💬	[4] P38, P38, P38, P38 💬 Retrograde endocannabinoid signaling × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Retrograde endocannabinoid signaling × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 94. Retrograde endocannabinoid signaling × Disease ID Name  8  Huntington disease;Huntington chorea;
95	RIG-I-like receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 RIG-I-like receptor signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 RIG-I-like receptor signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 95. RIG-I-like receptor signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
96	RIG-I-like receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 RIG-I-like receptor signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 RIG-I-like receptor signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 96. RIG-I-like receptor signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
97	Salmonella infection 💬	[4] P38, P38, P38, P38 💬 Salmonella infection × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Salmonella infection × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 97. Salmonella infection × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
98	Salmonella infection 💬	[4] P38, P38, P38, P38 💬 Salmonella infection × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Salmonella infection × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 98. Salmonella infection × Disease ID Name  8  Huntington disease;Huntington chorea;
99	Shigellosis 💬	[4] P38, P38, P38, P38 💬 Shigellosis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Shigellosis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 99. Shigellosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
100	Shigellosis 💬	[4] P38, P38, P38, P38 💬 Shigellosis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Shigellosis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 100. Shigellosis × Disease ID Name  8  Huntington disease;Huntington chorea;
101	Signaling pathways regulating pluripotency of stem cells 💬	[4] P38, P38, P38, P38 💬 Signaling pathways regulating pluripotency of stem cells × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Signaling pathways regulating pluripotency of stem cells × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 101. Signaling pathways regulating pluripotency of stem cells × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
102	Signaling pathways regulating pluripotency of stem cells 💬	[4] P38, P38, P38, P38 💬 Signaling pathways regulating pluripotency of stem cells × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Signaling pathways regulating pluripotency of stem cells × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 102. Signaling pathways regulating pluripotency of stem cells × Disease ID Name  8  Huntington disease;Huntington chorea;
103	Sphingolipid signaling pathway 💬	[4] P38, P38, P38, P38 💬 Sphingolipid signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Sphingolipid signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 102. Signaling pathways regulating pluripotency of stem cells × Disease ID Name  8  Huntington disease;Huntington chorea;
104	Sphingolipid signaling pathway 💬	[4] P38, P38, P38, P38 💬 Sphingolipid signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Sphingolipid signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 104. Sphingolipid signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
105	T cell receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 T cell receptor signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 T cell receptor signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 104. Sphingolipid signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
106	T cell receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 T cell receptor signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 T cell receptor signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 106. T cell receptor signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
107	Th1 and Th2 cell differentiation 💬	[4] P38, P38, P38, P38 💬 Th1 and Th2 cell differentiation × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Th1 and Th2 cell differentiation × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 107. Th1 and Th2 cell differentiation × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
108	Th1 and Th2 cell differentiation 💬	[4] P38, P38, P38, P38 💬 Th1 and Th2 cell differentiation × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Th1 and Th2 cell differentiation × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 108. Th1 and Th2 cell differentiation × Disease ID Name  8  Huntington disease;Huntington chorea;
109	Th17 cell differentiation 💬	[4] P38, P38, P38, P38 💬 Th1 and Th2 cell differentiation × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Th17 cell differentiation × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 108. Th1 and Th2 cell differentiation × Disease ID Name  8  Huntington disease;Huntington chorea;
110	Th17 cell differentiation 💬	[4] P38, P38, P38, P38 💬 Th17 cell differentiation × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Th17 cell differentiation × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 110. Th17 cell differentiation × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
111	Thermogenesis 💬	[4] P38, P38, P38, P38 💬 Thermogenesis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Thermogenesis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 110. Th17 cell differentiation × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
112	Thermogenesis 💬	[4] P38, P38, P38, P38 💬 Thermogenesis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Thermogenesis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 112. Thermogenesis × Disease ID Name  8  Huntington disease;Huntington chorea;
113	TNF signaling pathway 💬	[4] P38, P38, P38, P38 💬 TNF signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 TNF signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 113. TNF signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
114	TNF signaling pathway 💬	[4] P38, P38, P38, P38 💬 TNF signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 TNF signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 114. TNF signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
115	Toll-like receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 Toll-like receptor signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Toll-like receptor signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 114. TNF signaling pathway × Disease ID Name  8  Huntington disease;Huntington chorea;
116	Toll-like receptor signaling pathway 💬	[4] P38, P38, P38, P38 💬 Toll-like receptor signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Toll-like receptor signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 116. Toll-like receptor signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
117	Toxoplasmosis 💬	[4] P38, P38, P38, P38 💬 Toxoplasmosis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Toxoplasmosis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 116. Toll-like receptor signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
118	Toxoplasmosis 💬	[4] P38, P38, P38, P38 💬 Toxoplasmosis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Toxoplasmosis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 118. Toxoplasmosis × Disease ID Name  8  Huntington disease;Huntington chorea;
119	Tuberculosis 💬	[4] P38, P38, P38, P38 💬 Tuberculosis × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Tuberculosis × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 119. Tuberculosis × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
120	Tuberculosis 💬	[4] P38, P38, P38, P38 💬 Tuberculosis × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Tuberculosis × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 120. Tuberculosis × Disease ID Name  8  Huntington disease;Huntington chorea;
121	VEGF signaling pathway 💬	[4] P38, P38, P38, P38 💬 VEGF signaling pathway × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 VEGF signaling pathway × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 120. Tuberculosis × Disease ID Name  8  Huntington disease;Huntington chorea;
122	VEGF signaling pathway 💬	[4] P38, P38, P38, P38 💬 VEGF signaling pathway × Name Full Name P38 P38 P38 P38	Losmapimod 💬 VEGF signaling pathway × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 122. VEGF signaling pathway × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;
123	Yersinia infection 💬	[4] P38, P38, P38, P38 💬 Yersinia infection × Name Full Name P38 P38 P38 P38	Neflamapimod 💬 Yersinia infection × Name Other Names Neflamapimod Neflamapimod (USAN/INN)	Neflamapimod	[1]  8  💬 123. Yersinia infection × Disease ID Name  8  Huntington disease;Huntington chorea;
124	Yersinia infection 💬	[4] P38, P38, P38, P38 💬 Yersinia infection × Name Full Name P38 P38 P38 P38	Losmapimod 💬 Yersinia infection × Name Other Names Losmapimod Losmapimod (USAN/INN)	Losmapimod	[2] 113, 222 💬 124. Yersinia infection × Disease ID Name 113 Muscular dystrophy;Dystrophinopathies;Duchenne muscular dystrophy;DMD;Becker muscular dystrophy;BMD;Limb-girdle muscular dystrophy;LGMD;Congenital muscular dystrophy;CMD;Fukuyama-type congenital muscular dystrophy;FCMD;Walker-Warburg syndrome;Muscle-eye-brain disease;α-dystroglycanopathy;Integrin α7 deficient CMD;CIntegrin α7 deficient ongenital muscular dystrophy;Merosin-deficient congenital muscular dystrophy;Ullrich congenital muscular dystrophy;Laminopathy;Rigid spine syndrome;Dynamin 2 deficient congenital muscular dystrophy;Telesonin-deficient congenital muscular dystrophy;Congenital muscular dystrophy with mitochondrial structural abnormalities;Facioscapulohumeral muscular dystrophy;FSMD;Myotonic dystrophy;Dystrophia myotonica;DM;Emery-Dreifuss muscular dystrophy;EDMD;Oculopharyngeal muscular dystrophy;OPMD;Myotilinopathy;Caveolinopathy;Limb gridle muscular dystrophy 1C;LGMD1C;Desminopathy;Sarcoglycanopathy; 222 Primary nephrotic syndrome;Minimal change nephrotic syndrome;MCNS;Membranous nephropathy;Focal segmental glomerulosclerosis;FSGS;Membranoproliferative glomerulonephritis;MPGN;

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