ZFIN Human Disease: autosomal dominant nonsyndromic deafness 40

OBO ID: DOID:0110566

Term Name:	autosomal dominant nonsyndromic deafness 40		Search Ontology:
Synonyms:	autosomal dominant deafness 40 DFNA40
Definition:	An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the CRYM gene on chromosome 16p12. https://www.ncbi.nlm.nih.gov/pubmed/12471561
References:	ICD10CM:H90.3 OMIM:616357
Ontology:	Human Disease ( DOID:0110566 )

Relationships

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

OTHER autosomal dominant nonsyndromic deafness 40 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CRYM	crym	Deafness, autosomal dominant 40	616357

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None