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:C156360, 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.