hereditary sensory neuropathy type 1E Disease Ontology Browser

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Disease Ontology Browser

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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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