Wikidata entity: Q4863247
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2293 | genetic association | ... | Q6459047 (LMNB2) | LMNB2 |
| P1995 | health specialty | ... | Q162606 (endocrinology) | endocrinology |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P138 | named after | ... | Q9160494 (Arthur Simons) | Arthur Simons |
| P138 | named after | ... | Q9179901 (Luis Barraquer Roviralta) | Luis Barraquer Roviralta |
| P1748 | NCI Thesaurus ID | String | C129723 | ??? |
| P279 | subclass of | ... | Q53661802 (partial lipodystrophy) | partial lipodystrophy |
| P279 | subclass of | ... | Q55785399 (developmental anomaly of metabolic origin) | developmental anomaly of metabolic origin |
| P279 | subclass of | ... | Q55789110 (acquired lipodystrophy) | acquired lipodystrophy |
| P279 | subclass of | ... | Q1538213 (lipodystrophy) | lipodystrophy |
| P279 | subclass of | ... | Q6139748 (progeroid syndrome) | progeroid syndrome |
| P557 | DiseasesDB | 9697 |
| P4317 | GARD rare disease ID | 10509 |
| P494 | ICD-10 ID | E88.1 |
| P4229 | ICD-10-CM | E88.1 |
| P7807 | ICD-11 ID (Foundation) | 2042663302 |
| P7329 | ICD-11 ID (MMS) | EF01.0 |
| P493 | ICD-9 ID | 272.6 |
| P3201 | Medical Dictionary for Regulatory Activities ID | 10024608 |
| P6694 | MeSH concept ID | M0562748 |
| P486 | MeSH descriptor ID | C562448 |
| P6366 | Microsoft Academic ID (discontinued) | 2781400161 |
| P5270 | Mondo ID | MONDO_0012104 |
| P1368 | National Library of Latvia ID | 000334377 |
| P492 | OMIM ID | 608709 |
| P492 | OMIM ID | 608709 |
| P1550 | Orphanet ID | 79087 |
| P4233 | PatientsLikeMe condition ID | barraquer-simons-syndrome |
| P2892 | UMLS CUI | C0220989 |
| P11430 | UniProt disease ID | DI-02142 |
| P11143 | WikiProjectMed ID | Barraquer–Simons syndrome |
Why not click here or view trends?
log id: 5921189