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Summary Literature (2)
DOID:0050548 - hereditary sensory neuropathy

Disease Ontology Definition:A neuropathy characterized by congenital insensitivity to pain resulting in ulceration to the fingers, tongue, lips, and other distal appendages.

Synonyms: congenital insensitivity to pain, familial dysautonomia, type II, hereditary sensory and autonomic neuropathy

Referenced OMIM:

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : ntrk1, sptlc2, kif1a, retreg1, dst, sptlc1, atl3, ngf, elp1

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): neuropathy (is_a)

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Version: 4.14.0
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