hereditary sensory neuropathy type 1B Disease Ontology Browser

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Disease Ontology Browser

hereditary sensory neuropathy type 1B (DOID:0070148)
Alliance: disease page
Synonyms: hereditary sensory neuropathy type IB; HSAN with cough and gastroesophageal reflux
Alt IDs: OMIM:608088, MESH:C564296, ORDO:139564, UMLS_CUI:C1842586
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.

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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