| 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 | ... | Q14890978 (HFE) | HFE |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C84764 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q200779 (genetic disease) | genetic disease |
| P279 | subclass of | ... | Q3144934 (hereditary haemochromatosis) | hereditary haemochromatosis |
| P6363 | WordLift URL | Url | None | ??? |
| P699 | Disease Ontology ID | DOID:0111029 |
| P11956 | Experimental Factor Ontology ID | 0006513 |
| P4317 | GARD rare disease ID | 10417 |
| P4229 | ICD-10-CM | E83.1 |
| P5270 | Mondo ID | MONDO_0021001 |
| P492 | OMIM ID | 235200 |
| P492 | OMIM ID | 235200 |
| P1550 | Orphanet ID | 465508 |
| P2892 | UMLS CUI | C5679990 |
| P11430 | UniProt disease ID | DI-01714 |
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log id: 2994176