autosomal dominant nonsyndromic deafness 20

Term ID

DOID:0110550

Synonyms

• autosomal dominant deafness 20
• DFNA20
• DFNA26

Definition

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset with high frequency progressive hearing loss and has_material_basis_in mutation in the ACTG1 gene on chromosome 17q25. https://www.ncbi.nlm.nih.gov/pubmed/13680526

References

• ICD10CM:H90.3
• OMIM:604717

Ontology

Human Disease   ( DOID:0110550 )