autosomal dominant nonsyndromic deafness 9

Term ID

DOID:0110593

Synonyms

• autosomal dominant deafness 9
• DFNA9

Definition

An autosomal dominant nonsyndromic deafness that is characterized by postlingual onset in the second decade with high frequency progressive hearing loss and has_material_basis_in mutation in the COCH gene on chromosome 14q12. https://www.ncbi.nlm.nih.gov/pubmed/9806553

References

• ICD10CM:H90.3
• OMIM:601369

Ontology

Human Disease   ( DOID:0110593 )