KEGG DRUG

Disease ID	Name
13	Multiple sclerosis/Neuromyelitis optica
19	Lysosomal storage disease
34	Neurofibromatosis
84	Sarcoidosis
85	Idiopathic interstitial pneumonia
88	Chronic thromboembolic pulmonary hypertension
90	Retinitis pigmentosa
254	Porphyria
296	Biliary atresia
310	Congenital anomalies syndrome

[0]

[1] OPRM1 💬

[1] 310 💬

[1] Egg

[2] 96, 310 💬

[1] 310 💬

[43] 2, 5, 6, 13, 17, 34, 35, 46, 49, 50, 53, 58, 63, 65, 68, 76, 84, 86, 91, 93, 95, 96, 97, 98, 11 ...

Disease ID	Name
2	Amyotrophic lateral sclerosis
5	Progressive supranuclear palsy
6	Parkinson disease
13	Multiple sclerosis/Neuromyelitis optica
17	Multiple system atrophy
34	Neurofibromatosis
35	Pemphigus
46	Malignant rheumatoid arthritis
49	Systemic lupus erythematosus
50	Dermatomyositis
53	Sjogren syndrome
58	Hypertrophic cardiomyopathy
63	Idiopathic thrombocytopenic purpura
65	Primary immunodeficiency
68	Ossification of the ligamentum flavum
76	Pituitary gonadotropin secretion hyperthyroidism
84	Sarcoidosis
86	Pulmonary arterial hypertension
91	Budd-Chiari syndrome
93	Primary biliary cholangitis
95	Autoimmune hepatitis
96	Crohn disease
97	Ulcerative colitis
98	Eosinophilic gastrointestinal disease
113	Muscular dystrophy
137	Focal cortical dysplasia
158	Tuberous sclerosis
162	Pemphigoid
167	Marfan syndrome
171	Wilson disease
193	Prader-Willi syndrome
218	Alport syndrome
222	Primary nephrotic syndrome
224	Purpura nephritis
226	Interstitial cystitis with Hunners ulcer
227	Osler disease
230	Alveolar hypoventilation syndrome
271	Ankylosing spondylitis
291	Hirschsprung disease, entire colon type
296	Biliary atresia
298	Hereditary pancreatitis
310	Congenital anomalies syndrome
318	Citrin deficiency

[6] 2, 6, 13, 97, 228, 310 💬

[1] HMGCR 💬

[11] 6, 34, 46, 79, 156, 160, 195, 206, 263, 280, 310 💬

Disease ID	Name
6	Parkinson disease
34	Neurofibromatosis
46	Malignant rheumatoid arthritis
79	Homozygous familial hypercholesterolemia
156	Rett syndrome
160	Congenital ichthyosis
195	Noonan syndrome
206	Fragile X syndrome
263	Cerebrotendinous xanthomatosis
280	Huge arteriovenous malformation with cervicofacial or limb lesion
310	Congenital anomalies syndrome

[1] HMGCR 💬

Disease ID	Name
6	Parkinson disease
13	Multiple sclerosis/Neuromyelitis optica
15	Inclusion body myositis
34	Neurofibromatosis
46	Malignant rheumatoid arthritis
49	Systemic lupus erythematosus
51	Scleroderma
66	IgA nephropathy
79	Homozygous familial hypercholesterolemia
86	Pulmonary arterial hypertension
89	Lymphangioleiomyomatosis
94	Primary sclerosing cholangitis
158	Tuberous sclerosis
160	Congenital ichthyosis
162	Pemphigoid
195	Noonan syndrome
265	Lipodystrophy
288	Autoimmune acquired coagulation factor deficiency
298	Hereditary pancreatitis
299	Cystic fibrosis
310	Congenital anomalies syndrome