hereditary sensory and autonomic neuropathy type 5

Summary

DOID:0070145 - hereditary sensory and autonomic neuropathy type 5

Disease Ontology Definition:A hereditary sensory neuropathy characterized by impaired pain and thermal perception in the extremities and selective reduction in small myelinated fibers that has_material_basis_in homozygous mutation in the NGF gene on chromosome 1p13.

Synonyms: hereditary sensory and autonomic neuropathy type V, HSAN5

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

: ngf

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0012092 - hereditary sensory and autonomic neuropathy type 5

MONDO:0012092 - hereditary sensory and autonomic neuropathy type 5

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

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

Parent(s): autosomal recessive disease (is_a), hereditary sensory neuropathy (is_a)