autosomal recessive nonsyndromic deafness 31

Term ID

DOID:0110490

Synonyms

• autosomal recessive deafness 31
• DFNB31

Definition

An autosomal recessive nonsyndromic deafness that is characterized by prelingual onset and has_material_basis_in mutation in the WHRN gene on chromosome 9q32. https://www.ncbi.nlm.nih.gov/pubmed/12833159

References

• ICD10CM:H90.3
• OMIM:607084

Ontology

Human Disease   ( DOID:0110490 )