| class of disease | Q112193867 |
| autosomal dominant disease | Q18553439 |
| benign adult familial myoclonic epilepsy | Q56014305 |
| P699 | Disease Ontology ID | DOID:0111690 |
| P2888 | exact match | http://www.orpha.net/ORDO/Orphanet_86814 |
| http://identifiers.org/doid/DOID:0111690 | ||
| http://purl.obolibrary.org/obo/DOID_0111690 | ||
| P665 | KEGG ID | H02213 |
| P486 | MeSH descriptor ID | C563399 |
| P5270 | Mondo ID | MONDO_0010985 |
| P492 | OMIM ID | 601068 |
| 601068 | ||
| P2892 | UMLS CUI | C1832841 |
| P11430 | UniProt disease ID | DI-05296 |
| P2293 | genetic association | SAMD12 | Q18057719 |
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