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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: 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 (12)

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.11
The Jackson Laboratory