All diseases

OMIM ID
604563
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2; CMT4B2
Alternative terms:
CHARCOT-MARIE-TOOTH DISEASE, WITH FOCALLY FOLDED MYELIN SHEATHS, AUTOSOMAL RECESSIVE, TYPE 4B2
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4B2 CHARCOT-MARIE-TOOTH DISEASE, TYPE 4B2, WITH EARLY-ONSET GLAUCOMA, INCLUDED
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 4B2, WITH EARLY-ONSET GLAUCOMA, INCLUDED
(∗) Location:
11p15.4  
(†) Associated OMIM genes:
SBF2  
(‡) Associated MGI genes:
Sbf2  

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