Wikidata entity: Q32139750
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | None | ??? |
| P2293 | genetic association | ... | Q14905729 (SCN5A) | SCN5A |
| P1995 | health specialty | ... | Q10379 (cardiology) | cardiology |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C137959 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q200779 (genetic disease) | genetic disease |
| P279 | subclass of | ... | Q653924 (long QT syndrome) | long QT syndrome |
| P279 | subclass of | ... | Q18553439 (autosomal dominant disease) | autosomal dominant disease |
| P699 | Disease Ontology ID | DOID:0110646 |
| P4317 | GARD rare disease ID | 3286 |
| P4229 | ICD-10-CM | I45.8 |
| P486 | MeSH descriptor ID | C565840 |
| P5270 | Mondo ID | MONDO_0011377 |
| P492 | OMIM ID | 603830 |
| P492 | OMIM ID | 603830 |
| P2892 | UMLS CUI | C1838527 |
| P2892 | UMLS CUI | C1859062 |
| P2892 | UMLS CUI | C3276240 |
| P2892 | UMLS CUI | C3276241 |
| P11430 | UniProt disease ID | DI-00681 |
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log id: 1957224