ZFIN Human Disease: autosomal dominant nonsyndromic deafness 4A

OBO ID: DOID:0110573

Term Name:	autosomal dominant nonsyndromic deafness 4A		Search Ontology:
Synonyms:	autosomal dominant deafness 4A DFNA4A
Definition:	An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with flat or gently sloping hearing audioprofiles and has_material_basis_in mutation in the MYH14 gene on chromosome 19q13.33. https://www.ncbi.nlm.nih.gov/pubmed/15015131
References:	ICD10CM:H90.3 OMIM:600652
Ontology:	Human Disease ( DOID:0110573 )

Relationships

is a type of:	autosomal dominant nonsyndromic deafness autosomal dominant nonsyndromic deafness Show first 5 Terms

OTHER autosomal dominant nonsyndromic deafness 4A PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
MYH14	myh14	Deafness, autosomal dominant 4A	600652

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None