All diseases

OMIM ID
118200
OMIM term:
CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1B; CMT1B
Alternative terms:
HEREDITARY MOTOR AND SENSORY NEUROPATHY I; HMSN I
HEREDITARY MOTOR AND SENSORY NEUROPATHY IB; HMSN IB
HMSN1
HMSN1B
CHARCOT-MARIE-TOOTH NEUROPATHY, TYPE 1B
CHARCOT-MARIE-TOOTH DISEASE, SLOW NERVE CONDUCTION TYPE, LINKED TO DUFFY
PERONEAL MUSCULAR ATROPHY
CHARCOT-MARIE-TOOTH DISEASE, AUTOSOMAL DOMINANT, WITH FOCALLY FOLDED MYELIN SHEATHS, TYPE 1B
(∗) Location:
1q23.3  
(†) Associated OMIM genes:
MPZ  
(‡) Associated MGI genes:
Mpz  

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