DOID:0070162 - hereditary sensory and autonomic neuropathy type 1
Disease Ontology Definition:A hereditary sensory neuropathy characterized by slowly progressing, prominent, predominantly distal sensory loss and autonomic disturbances with juvenile or adult onset and autosomal dominant inheritance.
Synonyms: HSAN1, hereditary sensory and autonomic neuropathy type I
|MONDO:0018213 - hereditary sensory and autonomic neuropathy type 1|
Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Xenbase Genes : atl1, sptlc2, sptlc1, atl3
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): hereditary sensory neuropathy (is_a)