|OBO ID: DOID:0070158|
|Term Name:||hereditary sensory neuropathy type 1E||Search Ontology:|
|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|
|Ontology:||Human Disease (DOID:0070158)|
|is a type of:||
OTHER hereditary sensory neuropathy type 1E PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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