hereditary sensory and autonomic neuropathy type 1

Summary

DOID:0070162 - hereditary sensory and autonomic neuropathy type 1

Disease Ontology Definition:A hereditary sensory and autonomic neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance.

Synonyms: hereditary sensory and autonomic neuropathy type I, HSAN1, hereditary sensory neuropathy type 1, hereditary sensory neuropathy type I, HSN1

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

: atl1, sptlc2, sptlc1, atl3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0018213 - hereditary sensory and autonomic neuropathy type 1

MONDO:0018213 - hereditary sensory and autonomic neuropathy type 1

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

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

Parent(s): hereditary sensory and autonomic neuropathy (is_a)