All diseases

OMIM ID
162400
OMIM term:
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IA; HSAN1A
Alternative terms:
HSAN IA
NEUROPATHY, HEREDITARY SENSORY, TYPE IA; HSN1A
HSN IA
NEUROPATHY, HEREDITARY SENSORY RADICULAR, AUTOSOMAL DOMINANT, TYPE 1A
(∗) Location:
9q22.31  
(†) Associated OMIM genes:
SPTLC1  
(‡) Associated MGI genes:

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