DISEASES

Disease-gene associations mined from literature

Human genes for hereditary sensory neuropathy type 1E

Hereditary sensory neuropathy type 1E [DOID:0070158]

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:  hereditary sensory neuropathy type 1E,  DOID:0070158,  familial sensory neuropathy type 1E,  hereditary sensory neuropathy type IE,  HSN1E ...