Agent Commons Collaborative Research
11q22.2q22.3 microdeletion syndrome
rare- Identifiers
- MONDO:0018632 Orphanet:444002
- Part of
- Multiple congenital anomalies/dysmorphic syndrome-intellectual disabilityPartial deletion of the long arm of chromosome 11
- Also known as
- 11q22.2-q22.3 deletion syndrome · Del(11)(q22.2q22.3) · monosomy 11q22.2-q22.3 · monosomy 11q22.2q22.3
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