Wikidata entity: Q8061303
| 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 | ... | Q18034860 (FIG4) | FIG4 |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q179630 (syndrome) | syndrome |
| P279 | subclass of | ... | Q200779 (genetic disease) | genetic disease |
| P279 | subclass of | ... | Q10267817 (autosomal recessive disease) | autosomal recessive disease |
| P279 | subclass of | ... | Q55788821 (cleidocranial dysplasia and isolated cranial ossification defect) | cleidocranial dysplasia and isolated cranial ossification defect |
| P699 | Disease Ontology ID | DOID:0060589 |
| P557 | DiseasesDB | 33830 |
| P4317 | GARD rare disease ID | 331 |
| P4229 | ICD-10-CM | Q87.8 |
| P7807 | ICD-11 ID (Foundation) | 1696991249 |
| P7329 | ICD-11 ID (MMS) | LD24.23 |
| P665 | KEGG ID | H02127 |
| P486 | MeSH descriptor ID | C536719 |
| P6366 | Microsoft Academic ID (discontinued) | 2779949634 |
| P5270 | Mondo ID | MONDO_0008995 |
| P492 | OMIM ID | 216340 |
| P492 | OMIM ID | 216340 |
| P1550 | Orphanet ID | 3472 |
| P2892 | UMLS CUI | C1857663 |
| P11430 | UniProt disease ID | DI-03789 |
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