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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H00869 |
Leukoencephalopathy with vanishing white matter Vanishing white matter disease Childhood ataxia with diffuse central nervous system hypomyelination (CACH) Cree leukoencephalopathy (CLE) |
Leukoencephalopathy with vanishing white matter (VWM), also referred to as childhood ataxia with diffuse central nervous system hypomyelination (CACH), is one of the most prevalent inherited childhood ... | Nervous system disease |
(VWM1) EIF2B1 [HSA:1967] [KO:K03239] (VWM2) EIF2B2 [HSA:8892] [KO:K03754] (VWM3) EIF2B3 [HSA:8891] [KO:K03241] (VWM4) EIF2B4 [HSA:8890] [KO:K03680] (VWM5) EIF2B5 [HSA:8893] [KO:K03240] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |