autosomal dominant nonsyndromic deafness 71

Term ID

DOID:0080267

Synonyms

Definition

An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the DMXL2 gene on chromosome 15q21. https://pubmed.ncbi.nlm.nih.gov/27657680/

References

• OMIM:617605

Ontology

Human Disease   ( DOID:0080267 )