OBO ID: DOID:0110590
Term Name: autosomal dominant nonsyndromic deafness 69 Search Ontology:
Synonyms:
  • autosomal dominant deafness 69
  • DCUA
  • DFNA69
  • unilateral or asymmetric congenital deafness
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in mutation in the KITLG gene on chromosome 12q21. https://www.ncbi.nlm.nih.gov/pubmed/26522471
References:
Ontology: Human Disease   (DOID:0110590)
OTHER autosomal dominant nonsyndromic deafness 69 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
KITLG Deafness, autosomal dominant 69, unilateral or asymmetric 616697
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None