autosomal recessive nonsyndromic deafness 3

Term ID

DOID:0110488

Synonyms

• autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3
• DFNB3
• NRSD3

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 MYO15A gene on chromosome 17p11. https://www.ncbi.nlm.nih.gov/pubmed/17851452

References

• ICD10CM:H90.3
• OMIM:600316

Ontology

Human Disease   ( DOID:0110488 )