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Summary Literature (0)
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

Referenced OMIM:
OMIM:608654 - NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE V; HSAN5

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : ngf

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive disease (is_a), hereditary sensory neuropathy (is_a)


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Version: 4.14.0
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