ZFIN Human Disease: autosomal dominant nonsyndromic deafness 13

OBO ID: DOID:0110545

Term Name:	autosomal dominant nonsyndromic deafness 13		Search Ontology:
Synonyms:	autosomal dominant deafness 13 DFNA13
Definition:	An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade of life with mid-frequency hearing loss and has_material_basis_in mutation in the COL11A2 gene on chromosome 6p21. https://www.ncbi.nlm.nih.gov/pubmed/10581026
References:	ICD10CM:H90.3 OMIM:601868
Ontology:	Human Disease ( DOID:0110545 )

Relationships

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

OTHER autosomal dominant nonsyndromic deafness 13 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
COL11A2	col11a2	Deafness, autosomal dominant 13	601868

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None