Term Name: Fanconi anemia complementation group T
Synonyms: FANCT
Definition: A Fanconi anemia that has_material_basis_in compound heterozygous mutation in the UBE2T gene on chromosome 1q32.
Ontology: Human Disease [DOID:0111081]   ( DOID:0111081 )

Relationships
is a type of: autosomal recessive disease Fanconi anemia
inverse disjoint_from: Fanconi anemia complementation group V