Wikidata entity: Q1348398
| P373 | Commons category | String | Cancer predisposition syndromes | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P1269 | facet of | ... | Q3739537 (oncogenomics) | oncogenomics |
| P1995 | health specialty | ... | Q162555 (oncology) | oncology |
| P31 | instance of | ... | Q3311537 (hereditary disorder) | hereditary disorder |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C3266 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q12078 (cancer) | cancer |
| P279 | subclass of | ... | Q200779 (genetic disease) | genetic disease |
| P279 | subclass of | ... | Q1117773 (inherited tumor) | inherited tumor |
| P279 | subclass of | ... | Q18205885 (causes of cancer) | causes of cancer |
| P279 | subclass of | ... | Q55789476 (neoplastic syndrome) | neoplastic syndrome |
| P279 | subclass of | ... | Q55789522 (rare genetic disease) | rare genetic disease |
| P910 | topic's main category | ... | Q8508748 (Category:Hereditary cancers) | Category:Hereditary cancers |
| P486 | MeSH descriptor ID | D009386 |
| P672 | MeSH tree code | C04.700 |
| P672 | MeSH tree code | C16.320.700 |
| P6366 | Microsoft Academic ID (discontinued) | 2777277851 |
| P6366 | Microsoft Academic ID (discontinued) | 2909191862 |
| P5270 | Mondo ID | MONDO_0015356 |
| P11902 | NCI Dictionary of Genetics Terms entry | family-cancer-syndrome |
| P691 | NL CR AUT ID | ph195813 |
| P10283 | OpenAlex ID | C2777277851 |
| P10283 | OpenAlex ID | C2909191862 |
| P1550 | Orphanet ID | 140162 |
| P2892 | UMLS CUI | C0027672 |
| P2892 | UMLS CUI | C5680672 |
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