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Metadata
ID	DOID:0111096
Name	Fanconi anemia complementation group O
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
Xrefs	MIM:613390
Synonyms	FANCO [EXACT]
Parent Relationships	is_a Fanconi anemia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance