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Disease Ontology Browser
hereditary sensory neuropathy (DOID:0050548)
Synonyms: congenital insensitivity to pain; familial dysautonomia, type II; hereditary sensory and autonomic neuropathy
Alt IDs: OMIM:162400, OMIM:201300, OMIM:256800, OMIM:256860, OMIM:310470, OMIM:608088, OMIM:608654, OMIM:613115, OMIM:613640, OMIM:613708, OMIM:614116, OMIM:614213, OMIM:614653, OMIM:615548, OMIM:615632, OMIM:616488
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 (10)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
05/16/2017
MGI 6.09
The Jackson Laboratory