OBO ID: DOID:0111085
Term Name: Fanconi anemia complementation group U Search Ontology:
Synonyms:
  • FANCU
Definition: A Fanconi anemia that has_material_basis_in homozygous mutation in the XRCC2 gene on chromosome 7q36. https://www.ncbi.nlm.nih.gov/pubmed/22232082
References:
Ontology: Human Disease   ( DOID:0111085 )
Relationships
is a type of:
OTHER Fanconi anemia complementation group U PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
XRCC2 ?Fanconi anemia, complementation group U 617247
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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