hereditary sensory neuropathy type 1E (DOID:0070158)
Alliance: disease page
Synonyms: hereditary sensory neuropathy type IE; HSN1E
Alt IDs: OMIM:614116, ICD10CM:G60.8, ORDO:456318
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.