Wikidata entity: Q18555220
| 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 | Ontology Lookup Service (OLS) | ??? |
| P2293 | genetic association | ... | Q14865761 (GPI) | GPI |
| P2293 | genetic association | ... | Q14877634 (G6PD) | G6PD |
| P1995 | health specialty | ... | Q103824 (hematology) | hematology |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q5160435 (congenital hemolytic anemia) | congenital hemolytic anemia |
| P279 | subclass of | ... | Q55787283 (disorder of glycolysis) | disorder of glycolysis |
| P279 | subclass of | ... | Q55789127 (hemolytic anemia due to a disorder of glycolytic enzymes) | hemolytic anemia due to a disorder of glycolytic enzymes |
| P699 | Disease Ontology ID | DOID:2861 |
| P11956 | Experimental Factor Ontology ID | 1000641 |
| P4229 | ICD-10-CM | D55.2 |
| P486 | MeSH descriptor ID | D000746 |
| P672 | MeSH tree code | C15.378.050.141.150.100 |
| P672 | MeSH tree code | C16.320.070.100 |
| P5270 | Mondo ID | MONDO_0013275 |
| P492 | OMIM ID | 206300 |
| P492 | OMIM ID | 206300 |
| P492 | OMIM ID | 206400 |
| P492 | OMIM ID | 206400 |
| P492 | OMIM ID | 613470 |
| P492 | OMIM ID | 613470 |
| P492 | OMIM ID | 300908 |
| P492 | OMIM ID | 300908 |
| P1550 | Orphanet ID | 712 |
| P2892 | UMLS CUI | C0002882 |
| P2892 | UMLS CUI | C3150730 |
| P2892 | UMLS CUI | C5680791 |
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