autosomal recessive nonsyndromic deafness 42

Term ID

DOID:0110500

Synonyms

• autosomal recessive deafness 42
• DFNB42

Definition

An autosomal recessive nonsyndromic deafness that has_material_basis_in mutation in the ILDR1 gene on chromosome 3q13. https://www.ncbi.nlm.nih.gov/pubmed/21255762

References

• ICD10CM:H90.3
• OMIM:609646

Ontology

Human Disease   ( DOID:0110500 )