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Disease Ontology Browser
hereditary sensory and autonomic neuropathy type 2 (DOID:0070161)
Alliance: disease page
Synonyms: hereditary sensory and autonomic neuropathy type II; HSAN2
Alt IDs: MESH:D002607, MESH:D009477, ORDO:970, UMLS_CUI:C0020072, UMLS_CUI:C0270914
Definition: A hereditary sensory neuropathy characterized by progressively reduced sensation to pain, temperature, and touch, loss of myelinated and unmyelinated fibers, and hypotonia with onset at birth or in early childhood.

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
12/17/2024
MGI 6.24 		The Jackson Laboratory