Wikidata entity: Q3043160
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | Disease Ontology - Institute for Genome Sciences @ University of Maryland | ??? |
| P2888 | exact match | Url | None | ??? |
| P1325 | external data available at URL | Url | None | ??? |
| P1552 | has characteristic | ... | Q63645073 (deficiency) | deficiency |
| P1995 | health specialty | ... | Q101929 (immunology) | immunology |
| P1692 | ICD-9-CM | String | 279.3 | ??? |
| P31 | instance of | ... | Q42303753 (designated intractable/rare disease) | designated intractable/rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C3131 | ??? |
| P1748 | NCI Thesaurus ID | String | C152105 | ??? |
| P1748 | NCI Thesaurus ID | String | C39725 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q3843811 (immune disorder) | immune disorder |
| P699 | Disease Ontology ID | DOID:612 |
| P10565 | Encyclopedia of China (Third Edition) ID | 548649 |
| P646 | Freebase ID | /m/0gzxdg |
| P2671 | Google Knowledge Graph ID | /g/11dyjs1tw |
| P3841 | Human Phenotype Ontology ID | HP:0002721 |
| P4229 | ICD-10-CM | D84.9 |
| P7807 | ICD-11 ID (Foundation) | 587326822 |
| P665 | KEGG ID | H01725 |
| P486 | MeSH descriptor ID | D000081207 |
| P672 | MeSH tree code | C16.320.798 |
| P672 | MeSH tree code | C20.673.795 |
| P5270 | Mondo ID | MONDO_0021094 |
| P691 | NL CR AUT ID | ph358653 |
| P492 | OMIM ID | 242850 |
| P492 | OMIM ID | 242850 |
| P10283 | OpenAlex ID | C2779019163 |
| P1550 | Orphanet ID | 101997 |
| P2892 | UMLS CUI | C0021051 |
| P11143 | WikiProjectMed ID | Primary immunodeficiency |
| P3471 | WikiSkripta article ID | 4131 |
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