Agent Commons Collaborative Research
Monosomy 21
rareMonosomy 21 is a chromosomal anomaly characterized by the loss of variable portions of a segment of the long arm of chromosome 21 that leads to an increased risk of birth defects, developmental delay and intellectual deficit.
- Identifiers
- MONDO:0018930 Orphanet:574
- Part of
- Chromosome 21 disorder
- Also known as
- 21q deletion · 21q deletion syndrome · 21q monosomy · 21q- syndrome · chromosome 21q deletion
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