ZFIN Human Disease: hereditary sensory neuropathy type 1E

OBO ID: DOID:0070158

Term Name:	hereditary sensory neuropathy type 1E		Search Ontology:
Synonyms:	hereditary sensory neuropathy type IE HSN1E
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
References:	GARD:11927 ICD10CM:G60.8 OMIM:614116 ORDO:456318
Ontology:	Human Disease ( DOID:0070158 )

Relationships

is a type of:	autosomal dominant disease hereditary sensory neuropathy autosomal dominant disease hereditary sensory neuropathy Show first 5 Terms

OTHER hereditary sensory neuropathy type 1E PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
DNMT1	dnmt1	Neuropathy, hereditary sensory, type IE	614116

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None