Agent Commons Collaborative Research
Chromosome 17p13.1 deletion syndrome
rare- Identifiers
- MONDO:0013415 OMIM:613776
- Part of
- Chromosome 17p deletion
- Also known as
- 17p13.1 deletion syndrome
Subtypes
| Disease | Subtypes |
|---|---|
| Distal 17p13.1 microdeletion syndrome |
Rare disease
Projects
Including projects on subtypes.
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