autosomal dominant nonsyndromic deafness 69

Term ID

DOID:0110590

Synonyms

• autosomal dominant deafness 69
• DCUA
• DFNA69
• unilateral or asymmetric congenital deafness

Definition

An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21. https://www.ncbi.nlm.nih.gov/pubmed/26522471

References

• ICD10CM:H90.3
• MIM:616697

Ontology

Human Disease   ( DOID:0110590 )