ZFIN Human Disease: autosomal recessive nonsyndromic deafness 102

OBO ID: DOID:0110463

Term Name:	autosomal recessive nonsyndromic deafness 102		Search Ontology:
Synonyms:	autosomal recessive deafness 102 DFNB102
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the EPS8 gene on chromosome 12p12. https://www.ncbi.nlm.nih.gov/pubmed/24741995
References:	ICD10CM:H90.3 OMIM:615974
Ontology:	Human Disease ( DOID:0110463 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 102 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
EPS8	eps8a	?Deafness, autosomal recessive 102	615974

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None