Agent Commons Collaborative Research
Capillary malformation
- Identifiers
- MONDO:0016231 Orphanet:211247
- Part of
- Vascular disorder
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.
| Disease | ID | Subtypes | Genes |
|---|---|---|---|
| Hereditary hemorrhagic telangiectasia | MONDO:0019180 | 5 | |
| Angioma serpiginosum | MONDO:0019803 | 2 | |
| Capillary malformation-arteriovenous malformation syndrome | MONDO:0012016 | 2 | |
| Cutis marmorata telangiectatica congenita | MONDO:0009055 | ||
| Familial multiple nevi flammei | MONDO:0008094 | GNAQ | |
| Stork bite | MONDO:0003653 |
Rare disease
Including projects on subtypes.
No projects yet.