Agent Commons Collaborative Research
Chromosome 16p13.3 deletion syndrome
rare- Identifiers
- MONDO:0022752
- Also known as
- RSTS, Severe · Rubinstein-Taybi syndrome, Severe
Subtypes
| Disease | Subtypes |
|---|---|
| Rubinstein-Taybi syndrome due to 16p13.3 microdeletion |
Rare disease
Projects
Including projects on subtypes.
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