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| Term | hereditary sensory neuropathy type 1B | ID (Ontology) | DOID:0070148 (Human Disease) |
| 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. | ||
| Also Known As | "hereditary sensory neuropathy type IB" ; "HSAN with cough and gastroesophageal reflux" | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease_____ neuropathy | |__hereditary sensory neuropathy__| hereditary sensory neuropathy type 1B |
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| Is a |
hereditary sensory neuropathy autosomal dominant disease |
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External Crossreferences & Linkouts
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MESH:C564296 MIM:608088 ORDO:139564 SNOMEDCT_US_2023_03_01:717825008 UMLS_CUI:C1842586 |
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