ZFIN Human Disease: autosomal recessive nonsyndromic deafness 22

OBO ID: DOID:0110480

Term Name:	autosomal recessive nonsyndromic deafness 22		Search Ontology:
Synonyms:	autosomal recessive deafness 22 DFNB22
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOA gene on chromosome 16p12. https://www.ncbi.nlm.nih.gov/pubmed/11972037
References:	ICD10CM:H90.3 OMIM:607039
Ontology:	Human Disease ( DOID:0110480 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 22 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
OTOA	otoa	Deafness, autosomal recessive 22	607039

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None