Wikidata entity: Q9366868
| P927 | anatomical location | ... | Q9655 (artery) | artery |
| 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 | ... | Q18030434 (ENPP1) | ENPP1 |
| P2293 | genetic association | ... | Q14916171 (ABCC6) | ABCC6 |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P1748 | NCI Thesaurus ID | String | C128805 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q18965518 (artery disease) | artery disease |
| P699 | Disease Ontology ID | DOID:0050644 |
| P4317 | GARD rare disease ID | 8380 |
| P7464 | Genetics Home Reference Conditions ID | generalized-arterial-calcification-of-infancy |
| P665 | KEGG ID | H01002 |
| P486 | MeSH descriptor ID | C537440 |
| P6366 | Microsoft Academic ID (discontinued) | 2776991945 |
| P5270 | Mondo ID | MONDO_0008817 |
| P492 | OMIM ID | 208000 |
| P492 | OMIM ID | 208000 |
| P492 | OMIM ID | 614473 |
| P492 | OMIM ID | 614473 |
| P1550 | Orphanet ID | 51608 |
| P4233 | PatientsLikeMe condition ID | arterial-calcification-of-infancy |
| P2892 | UMLS CUI | C1859727 |
| P2892 | UMLS CUI | C1859728 |
| P11430 | UniProt disease ID | DI-01806 |
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log id: 5406259