- OMIM ID
-
608088
- OMIM term:
- NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE I, WITH COUGH AND GASTROESOPHAGEAL REFLUX
- Alternative terms:
-
NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IB; HSAN1B
NEUROPATHY, HEREDITARY SENSORY, TYPE IB; HSN1B
- (∗) Location:
- 3p24-p22
- (†) Associated OMIM genes:
- (‡) Associated MGI genes:
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