autosomal recessive nonsyndromic deafness 101

Term ID

DOID:0110462

Synonyms

• autosomal recessive deafness 101
• DFNB101

Definition

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the GRXCR2 gene on chromosome 5q32. https://www.ncbi.nlm.nih.gov/pubmed/24619944

References

• ICD10CM:H90.3
• OMIM:615837

Ontology

Human Disease   ( DOID:0110462 )