ZFIN Human Disease: autosomal recessive nonsyndromic deafness 21

OBO ID: DOID:0110479

Term Name:	autosomal recessive nonsyndromic deafness 21		Search Ontology:
Synonyms:	autosomal recessive deafness 21 DFNB21
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 TECTA gene on chromosome 11q23.3. https://www.ncbi.nlm.nih.gov/pubmed/9949200
References:	ICD10CM:H90.3 OMIM:603629
Ontology:	Human Disease ( DOID:0110479 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 21 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TECTA	tecta	Deafness, autosomal recessive 21	603629

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None