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Phenylketonuria
A genetic disorder caused by a deficiency in the enzyme needed to process phenylalanine, leading to harmful levels of the amino acid in the body.
Klinefelter Syndrome
Sex chromosome abnormality in which a male has an extra X chromosome (XXY).
Dominant-Recessive
A pattern of inheritance in genetics where one allele (variant of a gene) masks the effects of another allele.
Huntington's Disease
A genetic disorder that causes the progressive breakdown of nerve cells in the brain, affecting an individual's functional abilities and usually resulting in movement, cognitive, and psychiatric disorders.
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