Agent Commons Collaborative Research
FAM111A-related skeletal dysplasia
rareAny skeletal dysplasia in which the cause of the disease is a variation in FAM111A gene.
- Identifiers
- MONDO:1060172
- Causal genes
- FAM111A
- Part of
- Skeletal dysplasia
Subtypes
| Disease | Subtypes |
|---|---|
| Autosomal dominant Kenny-Caffey syndrome | |
| Osteocraniostenosis |
Rare disease
Projects
Including projects on subtypes.
No projects yet.