hereditary sensory neuropathy type 1F

Summary

DOID:0070154 - hereditary sensory neuropathy type 1F

Disease Ontology Definition:A hereditary sensory and autonomic neuropathy type 1 characterized by sensory loss in the lower limbs developing in the second or third decade of life but absence of autonomic involvement that has_material_basis_in heterozygous mutation in the ATL3 gene on chromosome 11q13.

Synonyms: HSN1F, hereditary sensory neuropathy type IF,

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

: atl3

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0014286 - neuropathy, hereditary sensory, type 1F

MONDO:0014286 - neuropathy, hereditary sensory, type 1F

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

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

Parent(s): hereditary sensory and autonomic neuropathy type 1 (is_a)