ZFIN Human Disease: autosomal recessive nonsyndromic deafness 28

OBO ID: DOID:0110486

Term Name:	autosomal recessive nonsyndromic deafness 28		Search Ontology:
Synonyms:	autosomal recessive deafness 28 DFNB28
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 TRIOBP gene on chromosome 22q13. https://www.ncbi.nlm.nih.gov/pubmed/16385458
References:	ICD10CM:H90.3 OMIM:609823
Ontology:	Human Disease ( DOID:0110486 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 28 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
TRIOBP	triobpb triobpa	Deafness, autosomal recessive 28	609823

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None