OBO ID: DOID:0111082
Term Name: Fanconi anemia complementation group L Search Ontology:
Synonyms:
  • FANCL
Definition: A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHF9 gene on chromosome 2p16. (2)
References:
Ontology: Human Disease   (DOID:0111082)
OTHER Fanconi anemia complementation group L PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
FANCL Fanconi anemia, complementation group L 614083
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None