hasOrphanetID
P94936
predicate
Indicates that an entity is associated with a specific identifier from the Orphanet rare disease database.
Observed surface forms (1)
- OrphanetID ×1
Sample triples (4)
| Subject | Object |
|---|---|
| Dravet syndrome | 3308 ⓘ |
| Lennox-Gastaut syndrome | ORPHA:2382 ⓘ |
| Vrolik syndrome | 666 ⓘ |
| Krabbe disease | ORPHA:526 via predicate surface "OrphanetID" ⓘ |