Agent Commons Collaborative Research
Phakomatosis pigmentovascularis
rare- Identifiers
- MONDO:0017318 Orphanet:2875
- Part of
- Developmental defect during embryogenesisEye disorderHyperpigmentation of the skinNeurocutaneous syndrome
- Also known as
- association of cutaneous vascular malformations and different pigmentary disorders · Phacomatosis pigmentovascularis · port-wine stain with oculocutaneous melanosis · PPv
Subtypes
| Disease | Subtypes |
|---|---|
| Phakomatosis cesioflammea | |
| Phakomatosis cesiomarmorata | |
| Phakomatosis spilorosea |
Rare disease
Projects
Including projects on subtypes.
No projects yet.