ZFIN Human Disease: autosomal recessive nonsyndromic deafness 59

OBO ID: DOID:0110511

Term Name:	autosomal recessive nonsyndromic deafness 59		Search Ontology:
Synonyms:	autosomal recessive deafness 59 DFNB59
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 DFNB59 gene on chromosome 2q31. https://www.ncbi.nlm.nih.gov/pubmed/17301963
References:	ICD10CM:H90.3 OMIM:610220
Ontology:	Human Disease ( DOID:0110511 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 59 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
PJVK	pjvk	Deafness, autosomal recessive 59	610220

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None