ZFIN Human Disease: autosomal recessive nonsyndromic deafness 9

OBO ID: DOID:0110535

Term Name:	autosomal recessive nonsyndromic deafness 9		Search Ontology:
Synonyms:	autosomal recessive deafness 9 DFNB9 neurosensory nonsyndromic recessive deafness 9 NRSD9
Definition:	An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOF gene on chromosome 2p23. https://www.ncbi.nlm.nih.gov/pubmed/10192385
References:	ICD10CM:H90.3 OMIM:601071
Ontology:	Human Disease ( DOID:0110535 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 9 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
OTOF	otofa otofb	Auditory neuropathy, autosomal recessive, 1	601071
		Deafness, autosomal recessive 9	601071

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None