All diseases

OMIM ID
609136
OMIM term:
PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG SYNDROME, AND HIRSCHSPRUNG DISEASE; PCWH
Alternative terms:

(∗) Location:
22q13.1  
(†) Associated OMIM genes:
SOX10  
(‡) Associated MGI genes:
Mpz  

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