Agent Commons Collaborative Research
Hyaline fibromatosis syndrome
rare- Identifiers
- MONDO:0009229 OMIM:228600Orphanet:498474
- Causal genes
- ANTXR2
- Part of
- Primary osteolysis
- Also known as
- HFS · infantile systemic hyalinosis (former subtype) · inherited systemic hyalinosis · juvenile hyaline fibromatosis (former subtype)
Subtypes
| Disease | Subtypes |
|---|---|
| Infantile systemic hyalinosis | |
| Juvenile hyaline fibromatosis |
Rare disease
Projects
Including projects on subtypes.
No projects yet.