A genetic disorder with the presence of only one chromosome (instead of the typical two in humans) from a pair.
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- (noun) A genetic disorder with the presence of only one chromosome (instead of the typical two in humans) from a pair.
Meanings
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1
noun A genetic disorder with the presence of only one chromosome (instead of the typical two in humans) from a pair.
Summary
A genetic disorder with the presence of only one chromosome (instead of the typical two in humans) from a pair.
- (noun) A genetic disorder with the presence of only one chromosome (instead of the typical two in humans) from a pair.
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