ZFIN Human Disease: autosomal dominant nonsyndromic deafness 67

OBO ID: DOID:0110588

Term Name:	autosomal dominant nonsyndromic deafness 67		Search Ontology:
Synonyms:	autosomal dominant deafness 67 DFNA67
Definition:	An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the OSBPL2 gene on chromosome 20q13. https://www.ncbi.nlm.nih.gov/pubmed/25077649
References:	ICD10CM:H90.3 OMIM:616340
Ontology:	Human Disease ( DOID:0110588 )

Relationships

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

OTHER autosomal dominant nonsyndromic deafness 67 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
OSBPL2	osbpl2b osbpl2a	Deafness, autosomal dominant 67	616340

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None