OBO ID: DOID:0070158 |
Term Name: | hereditary sensory neuropathy type 1E | Search Ontology: | |
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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. https://www.ncbi.nlm.nih.gov/pubmed/21532572 | ||
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Ontology: | Human Disease ( DOID:0070158 ) |
OTHER hereditary sensory neuropathy type 1E PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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