All diseases

OMIM ID
605253
OMIM term:
NEUROPATHY, CONGENITAL HYPOMYELINATING
Alternative terms:
CONGENITAL HYPOMYELINATING NEUROPATHY; CHN
HYPOMYELINATION, SEVERE CONGENITAL
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4E; CMT4E
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4E
(∗) Location:
10q21.3   1q23.3  
(†) Associated OMIM genes:
EGR2   MPZ  
(‡) Associated MGI genes:
Egr2  

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