Wikidata entity: Q56137331
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P828 | has cause | ... | Q504558 (triploidy) | triploidy |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P1692 | ICD-9-CM | String | 758.89 | ??? |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C85204 | ??? |
| P279 | subclass of | ... | Q200779 (genetic disease) | genetic disease |
| P279 | subclass of | ... | Q55786310 (syndromic obesity) | syndromic obesity |
| P279 | subclass of | ... | Q55789222 (chromosomal anomaly with cataract) | chromosomal anomaly with cataract |
| P557 | DiseasesDB | 32658 |
| P4317 | GARD rare disease ID | 5295 |
| P4229 | ICD-10-CM | Q92.7 |
| P7807 | ICD-11 ID (Foundation) | 1900317965 |
| P7329 | ICD-11 ID (MMS) | LD42.0 |
| P486 | MeSH descriptor ID | D057885 |
| P672 | MeSH tree code | C23.550.210.702.500 |
| P672 | MeSH tree code | G05.365.590.175.677.500 |
| P672 | MeSH tree code | G05.700.740.500 |
| P6366 | Microsoft Academic ID (discontinued) | 2778419287 |
| P5270 | Mondo ID | MONDO_0018067 |
| P1550 | Orphanet ID | 3376 |
| P2892 | UMLS CUI | C0333693 |
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