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| Entry | Name | Description | Category | Pathway | Gene |
|---|---|---|---|---|---|
| H02357 | Congenital hypomyelinating neuropathy | Congenital hypomyelinating neuropathy (CHN) is a rare congenital neuropathy, often accompanied by arthrogryposis, that is characterized by prenatal onset, areflexia, hypotonia, hypomyelination, and slowed ... | Nervous system disease |
(CHN1) EGR2 [HSA:1959] [KO:K12496] (CHN2) MPZ [HSA:4359] [KO:K06770] (CHN3) CNTNAP1 [HSA:8506] [KO:K07379] |
| [ KEGG | DISEASE | DRUG | MEDICUS ] |