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hereditary sensory and autonomic neuropathy

Disease Summary
Associated Targets (41)
Tbio

26

Tchem

8

Tclin

7


GARD Rare
Mondo Description An instance of sensory peripheral neuropathy that is caused by an inherited modification of the individual's genome.
Disease Ontology Description A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages.
Mondo Term and Equivalent IDs
MONDO:0015364:  hereditary sensory and autonomic neuropathy
COHD:380398: 
DC:0000323: 
GARD:0012688: 
ICD9:356.2: 
MESH:D009477: 
NCIT:C125386: 
OMIMPS:162400: 
Orphanet:140471: 
SCTID:11442006: 
UMLS:C0027889: