Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
DOID:0070155 - hereditary sensory and autonomic neuropathy type 2A

Disease Ontology Definition:A hereditary sensory and autonomic neuropathy type 2 characterized by progressive sensory neuropathy with onset in childhood that has_material_basis_in mutation in the HSN2 isoform of the WNK1 gene on chromosome 12p13.

Synonyms: hereditary sensory and autonomic neuropathy type IIA, HSAN2A

Xenbase Genes : wnk1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0024309 - neuropathy, hereditary sensory and autonomic, type 2A


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 and autonomic neuropathy type 2 (is_a)