Wikidata entity: Q21124507
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | None | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2293 | genetic association | ... | Q18052026 (SGO1) | SGO1 |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q179630 (syndrome) | syndrome |
| P279 | subclass of | ... | Q55785258 (genetic cardiac rhythm disease) | genetic cardiac rhythm disease |
| P279 | subclass of | ... | Q55785596 (rare genetic intestinal disease) | rare genetic intestinal disease |
| P699 | Disease Ontology ID | DOID:0060339 |
| P4317 | GARD rare disease ID | 12281 |
| P4229 | ICD-10-CM | K59.8 |
| P665 | KEGG ID | H02122 |
| P5270 | Mondo ID | MONDO_0014528 |
| P492 | OMIM ID | 616201 |
| P492 | OMIM ID | 616201 |
| P1550 | Orphanet ID | 435988 |
| P2892 | UMLS CUI | C4015474 |
| P11430 | UniProt disease ID | DI-04314 |
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log id: 5182217