autosomal recessive nonsyndromic deafness 9

Term ID

DOID:0110535

Synonyms

• autosomal recessive deafness 9
• DFNB9
• neurosensory nonsyndromic recessive deafness 9
• NRSD9

Definition

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset with usually severe to profound, stable hearing loss and has_material_basis_in mutation in the OTOF gene on chromosome 2p23. https://www.ncbi.nlm.nih.gov/pubmed/10192385

References

• ICD10CM:H90.3
• OMIM:601071

Ontology

Human Disease   ( DOID:0110535 )