Search Ontology:
Human Disease

Fanconi anemia complementation group O

Term ID
DOID:0111096
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 Pages
Alliance (1)
Genes Involved
Zebrafish Models
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