OBO ID: DOID:0111088
Term Name: Fanconi anemia complementation group F Search Ontology:
Synonyms:
  • FANCF
Definition: A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCF gene on chromosome 11p15. https://www.ncbi.nlm.nih.gov/pubmed/10615118
References:
Ontology: Human Disease   (DOID:0111088)
OTHER Fanconi anemia complementation group F PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FANCF Fanconi anemia, complementation group F 603467
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None