autosomal recessive nonsyndromic deafness 66

Term ID

DOID:0110517

Synonyms

• autosomal recessive deafness 66
• DFNB66

Definition

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the DCDC2 gene on chromosome 6p22. https://www.ncbi.nlm.nih.gov/pubmed/25601850

References

• ICD10CM:H90.3
• OMIM:610212

Ontology

Human Disease   ( DOID:0110517 )