autosomal recessive nonsyndromic deafness 61

Term ID

DOID:0110513

Synonyms

• autosomal recessive deafness 61
• DFNB61

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 SLC26A5 gene on chromosome 7q22. https://www.ncbi.nlm.nih.gov/pubmed/12719379

References

• ICD10CM:H90.3
• OMIM:613865

Ontology

Human Disease   ( DOID:0110513 )