ZFIN Human Disease: autosomal recessive nonsyndromic deafness 93

OBO ID: DOID:0110537

Term Name:	autosomal recessive nonsyndromic deafness 93		Search Ontology:
Synonyms:	autosomal recessive deafness 93 DFNB93
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the CABP2 gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/22981119
References:	ICD10CM:H90.3 OMIM:614899
Ontology:	Human Disease ( DOID:0110537 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 93 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CABP2	cabp2a cabp2b	Deafness, autosomal recessive 93	614899

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None