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Disease Ontology Browser
hereditary sensory and autonomic neuropathy (DOID:0050548)
Alliance: disease page
Synonyms: hereditary sensory neuropathy; HSAN; HSN
Alt IDs: ICD10CM:G60.8, MESH:D009477, OMIM:PS162400, ORDO:140471, UMLS_CUI:C0027889
Definition: A neuropathy characterized by axonal atrophy and degeneration, exclusively or predominantly affecting the sensory neurons, and variable autonomic dysfunction. Loss of pain and temperature sensation is an early and predominant, but not universal, symptom.

Disease References using Mouse Models (18)
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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Send questions and comments to User Support. 		last database update
04/14/2026
MGI 6.24 		The Jackson Laboratory