autosomal dominant nonsyndromic deafness 73

Term ID

DOID:0080269

Synonyms

Definition

An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the PTPRQ gene on chromosome 12q21. https://pubmed.ncbi.nlm.nih.gov/29309402/

References

• OMIM:617663

Ontology

Human Disease   ( DOID:0080269 )