OBO ID: DOID:0080268
Term Name: autosomal dominant nonsyndromic deafness 72 Search Ontology:
Synonyms:
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the SLC44A4 gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/28013291/
References:
Ontology: Human Disease   ( DOID:0080268 )
OTHER autosomal dominant nonsyndromic deafness 72 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC44A4 ?Deafness, autosomal dominant 72 617606
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None