ZFIN Human Disease: autosomal recessive nonsyndromic deafness 106

OBO ID: DOID:0080261

OBO ID: DOID:0080261

Term Name:	autosomal recessive nonsyndromic deafness 106	Search Ontology:
Synonyms:
Definition:	An autosomal recessive nonsyndromic deafness that has_material_basis_in homozygous mutation in the EPS8L2 gene on chromosome 11p15. https://pubmed.ncbi.nlm.nih.gov/26282398/
References:	OMIM:617637
Ontology:	Human Disease ( DOID:0080261 )

Relationships

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

OTHER autosomal recessive nonsyndromic deafness 106 PAGES

Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
EPS8L2	eps8l2	Deafness autosomal recessive 106	617637

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None