OBO ID: DOID:0111096
Term Name: Fanconi anemia complementation group O Search Ontology:
Synonyms:
  • FANCO
Definition: A Fanconi anemia that has_material_basis_in homozygous mutation in the RAD51C gene on chromosome 17q21-q24. https://www.ncbi.nlm.nih.gov/pubmed/20400963
References:
Ontology: Human Disease   ( DOID:0111096 )
Relationships
is a type of:
OTHER Fanconi anemia complementation group O PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
RAD51C Fanconi anemia, complementation group O 613390
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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