Wikidata entity: Q649602
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P1325 | external data available at URL | Url | None | ??? |
| P2293 | genetic association | ... | Q15319726 (ARX) | ARX |
| P2293 | genetic association | ... | Q18031400 (SCN8A) | SCN8A |
| P1995 | health specialty | ... | Q83042 (neurology) | neurology |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q42303753 (designated intractable/rare disease) | designated intractable/rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C116552 | ??? |
| P1748 | NCI Thesaurus ID | String | C188139 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q18553412 (neonatal period electroclinical syndrome) | neonatal period electroclinical syndrome |
| P279 | subclass of | ... | Q18555095 (infantile epileptic encephalopathy) | infantile epileptic encephalopathy |
| P279 | subclass of | ... | Q21694579 (childhood onset epileptic encephalopathy) | childhood onset epileptic encephalopathy |
| P699 | Disease Ontology ID | DOID:0050709 |
| P557 | DiseasesDB | 33878 |
| P646 | Freebase ID | /m/03d3f_w |
| P4317 | GARD rare disease ID | 9255 |
| P494 | ICD-10 ID | G40.4 |
| P7807 | ICD-11 ID (Foundation) | 1575860860 |
| P6366 | Microsoft Academic ID (discontinued) | 2780424539 |
| P5270 | Mondo ID | MONDO_0013801 |
| P492 | OMIM ID | 308350 |
| P492 | OMIM ID | 308350 |
| P1550 | Orphanet ID | 1934 |
| P2892 | UMLS CUI | C3281191 |
| P11143 | WikiProjectMed ID | Ohtahara syndrome |
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log id: 6188223