Wikidata entity: Q6139748
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P279 | subclass of | ... | Q200779 (genetic disease) | genetic disease |
| P279 | subclass of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P780 | symptoms and signs | ... | Q2070979 (senescence) | senescence |
| P780 | symptoms and signs | ... | Q105723518 (Prematurely aged appearance) | Prematurely aged appearance |
| P910 | topic's main category | ... | Q8795300 (Category:Progeroid syndromes) | Category:Progeroid syndromes |
| P2581 | BabelNet ID | 14105761n |
| P2581 | BabelNet ID | 14105761n |
| P646 | Freebase ID | /m/0dpvyc |
| P7807 | ICD-11 ID (Foundation) | 1520135105 |
| P7329 | ICD-11 ID (MMS) | LD2B |
| P3827 | JSTOR topic ID (archived) | premature-aging |
| P8408 | KBpedia ID | ProgeroidSyndrome |
| P486 | MeSH descriptor ID | D019588 |
| P672 | MeSH tree code | C23.888.069 |
| P6366 | Microsoft Academic ID (discontinued) | 2778113432 |
| P5270 | Mondo ID | MONDO_0015333 |
| P349 | NDL Authority ID | 01120054 |
| P10283 | OpenAlex ID | C2909947164 |
| P1550 | Orphanet ID | 139033 |
| P1550 | Orphanet ID | 363245 |
| P2892 | UMLS CUI | C0231341 |
| P2892 | UMLS CUI | C5680983 |
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log id: 5987496