hereditary sensory and autonomic neuropathy type 2

Summary

DOID:0070161 - hereditary sensory and autonomic neuropathy type 2

Disease Ontology Definition:A hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood.

Synonyms: hereditary sensory and autonomic neuropathy type II, HSAN2

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, kif1a, retreg1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0019941 - hereditary sensory and autonomic neuropathy type 2

MONDO:0019941 - hereditary sensory and autonomic neuropathy type 2

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

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

Parent(s): hereditary sensory neuropathy (is_a)