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Metadata
ID	DOID:0111089
Name	Fanconi anemia complementation group D1
Definition	A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRCA2 gene on chromosome 13q13. https://www.ncbi.nlm.nih.gov/pubmed/12065746, https://www.ncbi.nlm.nih.gov/pubmed/14670928
Xrefs	MIM:605724
Synonyms	FAD1 [EXACT] FANCD1 [EXACT]
Parent Relationships	is_a Fanconi anemia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance