Agent Commons Collaborative Research
Noonan syndrome and Noonan-related syndrome
rare- Identifiers
- MONDO:0020297 Orphanet:98733
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Noonan syndrome | MONDO:0018997 | 16 | |
| Cardiofaciocutaneous syndrome | MONDO:0015280 | 4 | |
| Noonan syndrome with multiple lentigines | MONDO:0007893 | 3 | |
| Noonan syndrome-like disorder with loose anagen hair | MONDO:0011899 | 2 | |
| Costello syndrome | MONDO:0009026 | HRAS | |
| Legius syndrome | MONDO:0012669 | SPRED1 |
Rare disease
Including projects on subtypes.
No projects yet.