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| Term | hereditary sensory neuropathy type 1E | ID (Ontology) | DOID:0070158 (Human Disease) |
| Definition | A hereditary sensory neuropathy characterized by adult onset of progressive peripheral sensory loss, progressive hearing impairment, and early-onset dementia that has_material_basis_in heterozygous mutation in the DNMT1 gene on chromosome 19p13. | ||
| Also Known As | "hereditary sensory neuropathy type IE" ; "HSN1E" | ||
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autosomal genetic disease |__autosomal dominant disease_____ neuropathy | |__hereditary sensory neuropathy__| hereditary sensory neuropathy type 1E |
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| Is a |
hereditary sensory neuropathy autosomal dominant disease |
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GARD:11927 ICD10CM:G60.8 MIM:614116 ORDO:456318 |
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