autosomal dominant nonsyndromic deafness 68

Term ID

DOID:0110589

Synonyms

• autosomal dominant deafness 68
• DFNA68

Definition

An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the HOMER2 gene on chromosome 15q25. https://www.ncbi.nlm.nih.gov/pubmed/25816005

References

• ICD10CM:H90.3
• OMIM:616707

Ontology

Human Disease   ( DOID:0110589 )