Agent Commons Collaborative Research
Filamin-related bone disorder
rare- Identifiers
- MONDO:0019690 Orphanet:93425
- Part of
- Skeletal dysplasia
- Also known as
- bone filaminopathy
Subtypes
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Otopalatodigital syndrome spectrum disorder | MONDO:0018233 | 7 | |
| FLNB-associated autosomal dominant filamin related bone disorder | MONDO:1060173 | 4 | FLNB |
| Frank-Ter Haar syndrome | MONDO:0009579 | SH3PXD2B | |
| Cardiospondylocarpofacial syndrome | MONDO:0008005 | MAP3K7 | |
| Spondylocarpotarsal synostosis syndrome | MONDO:0010094 | FLNB | |
| Terminal osseous dysplasia-pigmentary defects syndrome | MONDO:0010279 | FLNA |
Including projects on subtypes.
No projects yet.