hereditary sensory and autonomic neuropathy

Summary

DOID:0050548 - hereditary sensory and autonomic neuropathy

Disease Ontology Definition:A neuropathy characterized by axonal atrophy and degeneration, exclusively or predominantly affecting the sensory neurons, and variable autonomic dysfunction. Loss of pain and temperature sensation is an early and predominant, but not universal, symptom.

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

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: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

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

Parent(s): neuropathy (is_a)