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MIM:605253 - NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE; CHN1
Xenbase Genes: egr2, mpz
Human Disease Resource: MIM
| MONDO:0011527 - Charcot-Marie-Tooth disease type 4E |
| DOID:0110195 - Charcot-Marie-Tooth disease type 4E |
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| MONDO:0011527 - Charcot-Marie-Tooth disease type 4E |
| DOID:0110195 - Charcot-Marie-Tooth disease type 4E |