ZFIN Human Disease: autosomal dominant nonsyndromic deafness 10

OBO ID: DOID:0110542

Term Name:	autosomal dominant nonsyndromic deafness 10		Search Ontology:
Synonyms:	autosomal dominant deafness 10 DFNA10
Definition:	An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the third or forth decade of life with a flat or gently downsloping audioprofiles and has_material_basis_in mutation in the EYA4 gene on chromosome 6q23. https://www.ncbi.nlm.nih.gov/pubmed/11159937
References:	ICD10CM:H90.3 OMIM:601316
Ontology:	Human Disease ( DOID:0110542 )

Relationships

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

OTHER autosomal dominant nonsyndromic deafness 10 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
EYA4	eya4	Deafness, autosomal dominant 10	601316

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None