Examlex
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Down Syndrome
A genetic disorder caused by the presence of all or part of a third copy of chromosome 21, characterized by developmental and intellectual delays.
Phenylketonuria
A genetic disorder characterized by the body's inability to break down the amino acid phenylalanine, leading to harmful levels in the body.
Phenylalanine
An essential amino acid important in the biosynthesis of proteins.
Recessive Gene
A type of gene that expresses its traits only when paired with an identical or similar gene, as opposed to a dominant gene that can express its traits when paired with a different gene.
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