hereditary sensory neuropathy type 1B

Summary

DOID:0070148 - hereditary sensory neuropathy type 1B

Disease Ontology Definition:A hereditary sensory neuropathy characterized by axonal neuropathy with distal sensory impairment, cough, and gastroesophageal reflux that has_material_basis_in variation in the chromosome region 3p24-p22.

Synonyms: HSAN with cough and gastroesophageal reflux, hereditary sensory neuropathy type IB,

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

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Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011961 - hereditary sensory and autonomic neuropathy type 1B

MONDO:0011961 - hereditary sensory and autonomic neuropathy type 1B

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), hereditary sensory neuropathy (is_a)