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Metadata
ID	DOID:0060978
Name	Fanconi anemia complementation group W
Definition	A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the RFWD3 gene on chromosome 16q23. https://pubmed.ncbi.nlm.nih.gov/28691929/
Xrefs	MIM:617784
Parent Relationships	is_a Fanconi anemia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance