autosomal recessive nonsyndromic deafness 2

Term ID

DOID:0110477

Synonyms

• autosomal recessive deafness 2
• DFNB2

Definition

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the MYO7A gene on chromosome 11q13. https://www.ncbi.nlm.nih.gov/pubmed/9171833

References

• ICD10CM:H90.3
• OMIM:600060

Ontology

Human Disease   ( DOID:0110477 )