Wikidata entity: Q727096
| P373 | Commons category | String | Congenital diseases and disorders | ??? |
| P1343 | described by source | ... | Q124737633 (Armenian Soviet Encyclopedia, vol. 6) | Armenian Soviet Encyclopedia, vol. 6 |
| P1343 | described by source | ... | Q20078554 (Great Soviet Encyclopedia (1926–1947)) | Great Soviet Encyclopedia (1926–1947) |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P1552 | has characteristic | ... | Q21953121 (congenital onset) | congenital onset |
| P1552 | has characteristic | ... | Q10862879 (congenital characteristic) | congenital characteristic |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P5008 | on focus list of Wikimedia project | ... | Q54439832 (WikiProject Zika Corpus) | WikiProject Zika Corpus |
| P461 | opposite of | ... | Q3621717 (acquired disorder) | acquired disorder |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P910 | topic's main category | ... | Q6313232 (Category:Congenital disorders) | Category:Congenital disorders |
| P7033 | Australian Educational Vocabulary ID | scot/11236 |
| P2581 | BabelNet ID | 00010673n |
| P2581 | BabelNet ID | 00010673n |
| P1617 | BBC Things ID | fe19f690-17cc-4daa-9e6b-fa3a49760ca8 |
| P268 | Bibliothèque nationale de France ID | 165378758 |
| P508 | BNCF Thesaurus ID | 5056 |
| P1036 | Dewey Decimal Classification | 616.043 |
| P1036 | Dewey Decimal Classification | 571.976 |
| P699 | Disease Ontology ID | DOID:0080015 |
| P557 | DiseasesDB | 28811 |
| P4746 | Elhuyar ZTH ID | 134393 |
| P1417 | Encyclopædia Britannica Online ID | science/congenital-disorder |
| P5437 | EuroVoc ID | 5714 |
| P646 | Freebase ID | /m/01vj_9 |
| P227 | GND ID | 4039561-3 |
| P2924 | Great Russian Encyclopedia Online ID (old version) | 3159677 |
| P7807 | ICD-11 ID (Foundation) | 1048408993 |
| P7329 | ICD-11 ID (MMS) | XB8M |
| P5063 | Interlingual Index ID | i113025 |
| P3827 | JSTOR topic ID (archived) | congenital-anomalies |
| P6385 | Krugosvet article (archived) | nauka_i_tehnika/biologiya/VROZHDENNIE_POROKI.html |
| P244 | Library of Congress authority ID | sh85000182 |
| P486 | MeSH descriptor ID | D009358 |
| P672 | MeSH tree code | C16 |
| P6366 | Microsoft Academic ID (discontinued) | 2779778371 |
| P5270 | Mondo ID | MONDO_0000839 |
| P12596 | museum-digital tag ID | 102382 |
| P12596 | museum-digital tag ID | 102106 |
| P2004 | NALT ID | 730 |
| P2004 | NALT ID | 26788 |
| P9495 | National Historical Museums of Sweden ID | term/1CFCABC3-C391-4FD8-94BF-A6B03D9F6E7B |
| P8189 | National Library of Israel J9U ID | 987007292967905171 |
| P1368 | National Library of Latvia ID | 000083534 |
| P691 | NL CR AUT ID | ph216736 |
| P10283 | OpenAlex ID | C2779778371 |
| P10283 | OpenAlex ID | C2992981700 |
| P10283 | OpenAlex ID | C3019607859 |
| P5082 | Store medisinske leksikon ID | misdannelse |
| P12086 | WikiKids ID | Aangeboren_afwijking |
| P11143 | WikiProjectMed ID | Birth defect |
| P8814 | WordNet 3.1 Synset ID | 14236994-n |
| P8814 | WordNet 3.1 Synset ID | 14488632-n |
| P13591 | Yale LUX ID | concept/94bad096-9f41-4d9a-8620-dde63246cfb9 |
| P8309 | Yle topic ID | 18-295969 |
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