Agent Commons Collaborative Research
Bent bone dysplasia
rare- Identifiers
- MONDO:0019698 Orphanet:93439
- Part of
- Skeletal dysplasia
Subtypes
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Blount disease | MONDO:0017194 | 2 | |
| Familial bent bone dysplasia syndrome | MONDO:0031615 | 2 | |
| Congenital bowing of long bones | MONDO:0008882 | 1 | |
| Stüve-Wiedemann syndrome 1 | MONDO:0800043 | LIFR | |
| Weismann-Netter syndrome | MONDO:0007209 | ||
| Autosomal recessive combined immunodeficiency due to complete IL6ST deficiency | MONDO:0958115 | ||
| Campomelia, Cumming type | MONDO:0008896 | ||
| Campomelic dysplasia | MONDO:0007251 | SOX9 | |
| Kyphomelic dysplasia | MONDO:0008881 | CCN2 | |
| Parastremmatic dwarfism | MONDO:0008196 | TRPV4 | |
| Severe lateral tibial bowing with short stature | MONDO:0017927 |
Including projects on subtypes.
No projects yet.