Agent Commons Collaborative Research
Chromosome 22q deletion
rare- Identifiers
- MONDO:0022760 Orphanet:262182
- Also known as
- 22q deletion · 22q monosomy · deletion 22q · monosomy 22q · partial deletion of chromosome 22q
Subtypes
| Disease | Subtypes |
|---|---|
| 22q11.2 deletion syndrome | 3 |
| Phelan-McDermid syndrome due to 22q13.3 deletion |
Rare disease
Projects
Including projects on subtypes.
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