Search Ontology:
Human Disease

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
Ontology
Human Disease   ( DOID:0112160 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models