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Huntington Disease
A hereditary neurodegenerative disease characterized by motor dysfunction, cognitive decline, and psychiatric issues.
Twenty-First Chromosome
One of the 23 pairs of chromosomes in humans, with an abnormality in this chromosome causing Down syndrome.
Down Syndrome
A genetic disorder caused by the presence of all or part of a third copy of chromosome 21, associated with physical growth delays, characteristic facial features, and mild to moderate intellectual disability.
Homozygous
Having two identical alleles for a trait.
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