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Summary Literature (0)
DOID:0070158 - hereditary sensory neuropathy type 1E


Disease 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.

Synonyms: HSN1E, hereditary sensory neuropathy type IE

Xenbase Genes : dnmt1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013584 - hereditary sensory neuropathy-deafness-dementia syndrome


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): hereditary sensory neuropathy (is_a)