autosomal recessive nonsyndromic deafness 59

Term ID

DOID:0110511

Synonyms

• autosomal recessive deafness 59
• DFNB59

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 DFNB59 gene on chromosome 2q31. https://www.ncbi.nlm.nih.gov/pubmed/17301963

References

• ICD10CM:H90.3
• OMIM:610220

Ontology

Human Disease   ( DOID:0110511 )