Wikidata entity: Q5160435
| 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 | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P1995 | health specialty | ... | Q103824 (hematology) | hematology |
| P1692 | ICD-9-CM | String | 282 | ??? |
| P1692 | ICD-9-CM | String | 282.9 | ??? |
| P667 | ICPC 2 ID | String | B78 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q112965645 (symptom or sign) | symptom or sign |
| P1748 | NCI Thesaurus ID | String | C34379 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q18967566 (congenital anemia) | congenital anemia |
| P279 | subclass of | ... | Q1145668 (hemolytic anemia) | hemolytic anemia |
| P910 | topic's main category | ... | Q7215597 (Category:Hereditary hemolytic anemias) | Category:Hereditary hemolytic anemias |
| P699 | Disease Ontology ID | DOID:589 |
| P4317 | GARD rare disease ID | 6167 |
| P3841 | Human Phenotype Ontology ID | HP:0004804 |
| P4229 | ICD-10-CM | D58.9 |
| P7807 | ICD-11 ID (Foundation) | 950429256 |
| P3827 | JSTOR topic ID (archived) | congenital-hemolytic-anemia |
| P486 | MeSH descriptor ID | D000745 |
| P672 | MeSH tree code | C15.378.071.141.150 |
| P672 | MeSH tree code | C16.320.070 |
| P6366 | Microsoft Academic ID (discontinued) | 2910179600 |
| P5270 | Mondo ID | MONDO_0015910 |
| P1550 | Orphanet ID | 182043 |
| P2892 | UMLS CUI | C0002881 |
| P2892 | UMLS CUI | C4020827 |
| P2892 | UMLS CUI | C5680605 |
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