Wikidata entity: Q18558086
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | None | ??? |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P1995 | health specialty | ... | Q162606 (endocrinology) | endocrinology |
| P1692 | ICD-9-CM | String | 270 | ??? |
| P1692 | ICD-9-CM | String | 270.9 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C97090 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q1758393 (inherited metabolic disorder) | inherited metabolic disorder |
| P699 | Disease Ontology ID | DOID:9252 |
| P4317 | GARD rare disease ID | 5793 |
| P4317 | GARD rare disease ID | 6770 |
| P4229 | ICD-10-CM | E72.9 |
| P486 | MeSH descriptor ID | D000592 |
| P672 | MeSH tree code | C16.320.565.100 |
| P672 | MeSH tree code | C18.452.648.100 |
| P5270 | Mondo ID | MONDO_0004736 |
| P1550 | Orphanet ID | 79062 |
| P2892 | UMLS CUI | C0002514 |
| P2892 | UMLS CUI | C0342666 |
| P2892 | UMLS CUI | C0750905 |
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log id: 5362074