autosomal recessive nonsyndromic deafness 37

Term ID

DOID:0110495

Synonyms

• autosomal recessive deafness 37
• DFNB37

Definition

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the MYO6 gene on chromosome 6q14. https://www.ncbi.nlm.nih.gov/pubmed/12687499

References

• ICD10CM:H90.3
• MIM:607821

Ontology

Human Disease   ( DOID:0110495 )