Congenital Disorder

Translocation, Genetic

AMW:DIS:230071

A type of chromosome aberration characterized by CHROMOSOME BREAKAGE and transfer of the broken-off portion to another location, often to a different chromosome.

Pathology clinical

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Translocation, Genetic has parent Chromosome Aberrations

Translocation, Genetic has parent Mutagenesis

Philadelphia Chromosome has parent Translocation, Genetic

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