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hereditary sensory and autonomic neuropathy type 5 (DOID:0070145)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type V; HSAN5
Alt IDs: OMIM:608654, MESH:D000699, MESH:D009477, NCI:C125386, ORDO:608654, UMLS_CUI:C0002768, UMLS_CUI:C0020075
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.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
02/18/2020
MGI 6.14
The Jackson Laboratory