autosomal dominant nonsyndromic deafness 6

Term ID

DOID:0110584

Synonyms

• autosomal dominant deafness 14
• autosomal dominant deafness 38
• autosomal dominant deafness 6
• DFNA14
• DFNA38
• DFNA6

Definition

An autosomal dominant nonsyndromic deafness that is characterized by prelingual onset and low frequency progressive hearing loss and has_material_basis_in mutation in the WFS1 gene on chromosome 4p16. (2)

References

• ICD10CM:H90.3
• OMIM:600965

Ontology

Human Disease   ( DOID:0110584 )