ZFIN Human Disease: autosomal recessive nonsyndromic deafness 35

OBO ID: DOID:0110493

Term Name:	autosomal recessive nonsyndromic deafness 35		Search Ontology:
Synonyms:	autosomal recessive deafness 35 DFNB35
Definition:	An autosomal recessive nonsyndromic deafness that is characterized severe to profound hearing loss and has_material_basis_in mutation in the ESRRB gene on chromosome 14q24. https://www.ncbi.nlm.nih.gov/pubmed/18179891
References:	ICD10CM:H90.3 OMIM:608565
Ontology:	Human Disease ( DOID:0110493 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 35 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
ESRRB	esrrb	Deafness, autosomal recessive 35	608565

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None