OBO ID: DOID:0112168
Term Name: autosomal dominant nonsyndromic deafness 77 Search Ontology:
Synonyms:
  • DFNA77
Definition: An autosomal dominant nonsyndromic deafness that has_material_basis_in heterozygous mutation in the ABCC1 gene on chromosome 16p13.11. https://pubmed.ncbi.nlm.nih.gov/31273342/
References:
Ontology: Human Disease   ( DOID:0112168 )
Relationships
is a type of:
OTHER autosomal dominant nonsyndromic deafness 77 PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
ABCC1 ?Deafness, autosomal dominant 77 618915
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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