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Disease Ontology Browser
hereditary sensory and autonomic neuropathy type 2 (DOID:0070161)
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Synonyms: hereditary sensory and autonomic neuropathy type II; hereditary sensory neuropathy type 2; hereditary sensory neuropathy type II; HSAN2; HSN2
Alt IDs: ORDO:970, UMLS_CUI:C0020072
Definition: A hereditary sensory and autonomic neuropathy characterized by progressive, primarily distal reduced sensation to pain, temperature, and touch with congenital to juvenile onset, autosomal recessive inheritance, and variable, limited autonomic and muscular dysfunction. Loss of sensation commonly results in Charcot joints, unnoticed lacerations, acral mutilations, and osteomyelitis.

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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03/31/2026
MGI 6.24 		The Jackson Laboratory