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Summary Literature (0)
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


In Mondo Disease Ontology:
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)