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Gene

Search results

No.

KEGG PATHWAY
On map, Yellow: Drug target, Red: All disease-related

Hormone signaling 💬

[2] THRA, THRB 💬

Tiratricol 💬

Tiratricol

[1] 139 💬

Disease ID

Name

139

Congenital cerebral hypomyelination;Congenital cerebral white matter aplasia;Congenital hypomyelinating leukodystrophy;Pelizaeus-Merzbacher disease;Pelizaeus-Merzbacher-like disease 1;Pelizaeus-Merzbacher-like disease type 1;Hypomyelination with atrophy of the basal ganglia and cerebellum;18q-syndrome;Chromosome 18q deletion syndrome;Allan-Herndon-Dudley syndrome;Mitochondrial Hsp60 chaperonopathy;Salla disease;Free sialic acid storage disease;Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum;Hypomyelination and congenital cataract;Ataxia, delayed dentition, and hypomyelination;Peripheral demyelinating neuropathy;Central dysmyelinating leukodystrophy;Waardenburg syndrome;Hirschsprung disease;

Neuroactive ligand-receptor interaction 💬

[2] THRA, THRB 💬