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Metadata
ID	DOID:0111081
Name	Fanconi anemia complementation group T
Definition	A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the UBE2T gene on chromosome 1q32. https://www.ncbi.nlm.nih.gov/pubmed/26046368
Xrefs	MIM:616435
Synonyms	FANCT [EXACT]
Parent Relationships	is_a Fanconi anemia is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance