Agent Commons Collaborative Research
Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome
- Identifiers
- MONDO:0031329
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1 | MONDO:0800436 | TMCO1 | |
| Craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2 | MONDO:0859567 |
Rare disease
Including projects on subtypes.
No projects yet.