autosomal recessive nonsyndromic deafness 16

Term ID

DOID:0110471

Synonyms

• autosomal recessive deafness 16
• DFNB16

Definition

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with severe to profound, stable hearing loss and has_material_basis_in mutation in the STRC gene on chromosome 15q15. https://www.ncbi.nlm.nih.gov/pubmed/11687802

References

• ICD10CM:H90.3
• OMIM:603720

Ontology

Human Disease   ( DOID:0110471 )