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

• OMIM:617637

Ontology

Human Disease   ( DOID:0080261 )