Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (2)
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 : 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


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): neuropathy (is_a)