hereditary sensory neuropathy

Summary

DOID:0050548 - hereditary sensory neuropathy

Disease Ontology Definition:A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages.

Synonyms: congenital insensitivity to pain, familial dysautonomia, type II, hereditary sensory and autonomic neuropathy,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: wnk1, ntrk1, atl1, sptlc2, prdm12, kif1a, dnmt1, retreg1, dst, sptlc1, atl3, ngf, elp1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0015364 - hereditary sensory and autonomic neuropathy

MONDO:0015364 - hereditary sensory and autonomic neuropathy

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): neuropathy (is_a)