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DOID:0070145 - hereditary sensory and autonomic neuropathy type 5
Disease Ontology Definition:A hereditary sensory neuropathy characterized by impaired pain and thermal perception in the extremities and selective reduction in small myelinated fibers that has_material_basis_in homozygous mutation in the NGF gene on chromosome 1p13.
Synonyms: HSAN5, hereditary sensory and autonomic neuropathy type V,
Echinobase Genes
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
MIM:608654 - neuropathy, hereditary sensory and autonomic, type v; hsan5 |
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
hereditary sensory neuropathy (is_a)