ZFIN Human Disease: autosomal recessive nonsyndromic deafness 48

OBO ID: DOID:0110505

Term Name:	autosomal recessive nonsyndromic deafness 48		Search Ontology:
Synonyms:	autosomal recessive deafness 48 DFNB48
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the CIB2 gene on chromosome 15q25. https://www.ncbi.nlm.nih.gov/pubmed/23023331
References:	ICD10CM:H90.3 OMIM:609439
Ontology:	Human Disease ( DOID:0110505 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 48 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CIB2	cib2	Deafness, autosomal recessive 48	609439

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None