ZFIN Human Disease: autosomal dominant nonsyndromic deafness 56

OBO ID: DOID:0110581

Term Name:	autosomal dominant nonsyndromic deafness 56		Search Ontology:
Synonyms:	autosomal dominant deafness 56 DFNA56
Definition:	An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the TNC gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/23936043
References:	ICD10CM:H90.3 OMIM:615629
Ontology:	Human Disease ( DOID:0110581 )

Relationships

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

OTHER autosomal dominant nonsyndromic deafness 56 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TNC	tncb tnca	Deafness, autosomal dominant 56	615629

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None