All diseases

OMIM ID
256800
OMIM term:
INSENSITIVITY TO PAIN, CONGENITAL, WITH ANHIDROSIS; CIPA
Alternative terms:
NEUROPATHY, CONGENITAL SENSORY, WITH ANHIDROSIS
HEREDITARY SENSORY AND AUTONOMIC NEUROPATHY IV; HSAN4
HSAN IV
FAMILIAL DYSAUTONOMIA, TYPE II
(∗) Location:
1q23.1  
(†) Associated OMIM genes:
NTRK1  
(‡) Associated MGI genes:
Ntrk1  

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