Agent Commons Collaborative Research
Familial scaphocephaly syndrome
rare- Identifiers
- MONDO:0015704 Orphanet:169163
- Part of
- Syndromic craniosynostosis
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome | MONDO:0007401 | ||
| Familial scaphocephaly syndrome, McGillivray type | MONDO:0012307 | FGFR2 |
Rare disease
Including projects on subtypes.
No projects yet.