ZFIN Human Disease: autosomal dominant nonsyndromic deafness 21

OBO ID: DOID:0110551

Term Name:	autosomal dominant nonsyndromic deafness 21		Search Ontology:
Synonyms:	autosomal dominant deafness 21 DFNA21
Definition:	An autosomal dominant nonsyndromic deafness that has_material_basis_in variation in the chromosome region 6p24.1-p22.3. https://www.ncbi.nlm.nih.gov/pubmed/10764236
References:	ICD10CM:H90.3 OMIM:607017
Ontology:	Human Disease ( DOID:0110551 )

Relationships

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

OTHER autosomal dominant nonsyndromic deafness 21 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
RIPOR2	ripor2	Deafness, autosomal dominant 21	607017

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None