- OMIM ID
-
201300
- OMIM term:
- NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IIA; HSAN2A
- Alternative terms:
-
HSAN IIA
NEUROPATHY, HEREDITARY SENSORY, TYPE IIA; HSN2A; HSN IIA
ACROOSTEOLYSIS, NEUROGENIC
ACROOSTEOLYSIS, GIACCAI TYPE
NEUROPATHY, HEREDITARY SENSORY RADICULAR, AUTOSOMAL RECESSIVE
MORVAN DISEASE
NEUROPATHY, PROGRESSIVE SENSORY, OF CHILDREN
NEUROPATHY, CONGENITAL SENSORY
- (∗) Location:
- 12p13.33
- (†) Associated OMIM genes:
- WNK1
- (‡) Associated MGI genes:
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