Wikidata entity: Q200779
| P2841 | age of onset | ... | Q118907676 (any age) | any age |
| P373 | Commons category | String | Genetic diseases and disorders | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | None | ??? |
| P828 | has cause | ... | Q7208 (pathology) | pathology |
| P828 | has cause | ... | Q5552256 (germline mutation) | germline mutation |
| P2354 | has list | ... | Q665092 (list of genetic disorders) | list of genetic disorders |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P1692 | ICD-9-CM | String | 799.89 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C3101 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P461 | opposite of | ... | Q3751709 (environmental disease) | environmental disease |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q3311537 (hereditary disorder) | hereditary disorder |
| P910 | topic's main category | ... | Q7031586 (Category:Genetic diseases and disorders) | Category:Genetic diseases and disorders |
| P9084 | ABC News topic ID | genetic-disorders |
| P7033 | Australian Educational Vocabulary ID | scot/16746 |
| P2581 | BabelNet ID | 00021810n |
| P2581 | BabelNet ID | 00021810n |
| P4255 | Banglapedia ID (English) | Genetic_Disorder |
| P1617 | BBC Things ID | 9b8e2ec0-66ac-4d5a-9eb5-966032dbb756 |
| P268 | Bibliothèque nationale de France ID | 119442366 |
| P508 | BNCF Thesaurus ID | 5047 |
| P5395 | Canadian Encyclopedia article ID | genetic-diseases |
| P5395 | Canadian Encyclopedia article ID | genetic-diseases |
| P1036 | Dewey Decimal Classification | 616.042 |
| P699 | Disease Ontology ID | DOID:630 |
| P1417 | Encyclopædia Britannica Online ID | science/genetic-disease |
| P11956 | Experimental Factor Ontology ID | 0000508 |
| P646 | Freebase ID | /m/03896 |
| P227 | GND ID | 4015106-2 |
| P3827 | JSTOR topic ID (archived) | genetic-disorders |
| P8408 | KBpedia ID | GeneticDisorder |
| P8313 | Lex ID | genetiske_sygdomme |
| P244 | Library of Congress authority ID | sh87001834 |
| P1149 | Library of Congress Classification | RB155.5-RB155.8 |
| P486 | MeSH descriptor ID | D030342 |
| P672 | MeSH tree code | C16.320 |
| P6366 | Microsoft Academic ID (discontinued) | 2778908642 |
| P5270 | Mondo ID | MONDO_0003847 |
| P2004 | NALT ID | 18968 |
| P8189 | National Library of Israel J9U ID | 987007529859105171 |
| P1368 | National Library of Latvia ID | 000083538 |
| P950 | National Library of Spain SpMaBN ID (BNE v1.0) | XX527199 |
| P10283 | OpenAlex ID | C2778908642 |
| P10283 | OpenAlex ID | C2908532627 |
| P10283 | OpenAlex ID | C2910788575 |
| P10283 | OpenAlex ID | C3018605307 |
| P2892 | UMLS CUI | C0019247 |
| P12800 | Vikidia article ID | fr:Maladie_génétique |
| P11143 | WikiProjectMed ID | Genetic disorder |
| P8814 | WordNet 3.1 Synset ID | 14174621-n |
| P13591 | Yale LUX ID | concept/84abfa16-5d48-4a54-bbf5-dd753c39eba9 |
| P2347 | YSO ID | 19997 |
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