autosomal dominant nonsyndromic deafness 79

Term ID

DOID:0112160

Synonyms

• DFNA79

Definition

An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the SCD5 gene on chromosome 4q21.22. https://pubmed.ncbi.nlm.nih.gov/31972369/

References

• OMIM:619086

Ontology

Human Disease   ( DOID:0112160 )