ZFIN Human Disease: autosomal dominant nonsyndromic deafness 27

OBO ID: DOID:0110556

Term Name:	autosomal dominant nonsyndromic deafness 27		Search Ontology:
Synonyms:	autosomal dominant deafness 27 DFNA27
Definition:	An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 4q12-q13.1. https://www.ncbi.nlm.nih.gov/pubmed/18279434
References:	ICD10CM:H90.3 OMIM:612431
Ontology:	Human Disease ( DOID:0110556 )

Relationships

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

OTHER autosomal dominant nonsyndromic deafness 27 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
REST	rest	Deafness, autosomal dominant 27	612431

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None