Congenital Disorder

Nondisjunction, Genetic

AMW:DIS:230064

The failure of homologous CHROMOSOMES or CHROMATIDS to segregate during MITOSIS or MEIOSIS with the result that one daughter cell has both of a pair of parental chromosomes or chromatids and the other has none.

Pathology clinical

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Nondisjunction, Genetic has parent Chromosome Aberrations

Uniparental Disomy has parent Nondisjunction, Genetic

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