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Human Disease

autosomal recessive nonsyndromic deafness 106

Term ID
DOID:0080261
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
Ontology
Human Disease   ( DOID:0080261 )
Relationships
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Genes Involved
Zebrafish Models