OMIMID
P68676
predicate
Indicates that an entity (typically a gene or disease) is associated with a specific OMIM (Online Mendelian Inheritance in Man) identifier in the OMIM database.
Observed surface forms (1)
- hasOMIMID ×2
Sample triples (9)
| Subject | Object |
|---|---|
| 5q13 (SMN1) | 600354 ⓘ |
| Angelman syndrome | 105830 ⓘ |
| C9orf72 | 614260 ⓘ |
| Dravet syndrome | 607208 via predicate surface "hasOMIMID" ⓘ |
|
HTT gene
surface form:
HTT
|
613004 ⓘ |
| Krabbe disease | 245200 ⓘ |
| SCN1A | 182389 ⓘ |
|
SMN1 gene
surface form:
SMN1
|
600354 ⓘ |
| Vrolik syndrome | 166210 via predicate surface "hasOMIMID" ⓘ |