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Disease Ontology Browser
hereditary sensory neuropathy (DOID:0050548)
Alliance: disease page
Synonyms: familial dysautonomia, type II; hereditary sensory and autonomic neuropathy
Alt IDs: MESH:D009477, OMIM:PS162400
Definition: A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages.

Disease References using Mouse Models (17)
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
10/29/2024
MGI 6.24 		The Jackson Laboratory