Wikidata entity: Q3501154
| P373 | Commons category | String | Larsen syndrome | ??? |
| P1889 | different from | ... | Q7234096 (postpericardiotomy syndrome) | postpericardiotomy syndrome |
| 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 | ... | Q17928818 (FLNB) | FLNB |
| P1692 | ICD-9-CM | String | 759.89 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P31 | instance of | ... | Q55789477 (head and neck disease) | head and neck disease |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q18553439 (autosomal dominant disease) | autosomal dominant disease |
| P279 | subclass of | ... | Q55785403 (rare developmental defect with connective tissue involvement) | rare developmental defect with connective tissue involvement |
| P279 | subclass of | ... | Q55785405 (orofacial clefting syndrome) | orofacial clefting syndrome |
| P279 | subclass of | ... | Q55788802 (filamin-related bone disorder) | filamin-related bone disorder |
| P279 | subclass of | ... | Q55788812 (primary bone dysplasia with multiple joint dislocations) | primary bone dysplasia with multiple joint dislocations |
| P699 | Disease Ontology ID | DOID:14764 |
| P557 | DiseasesDB | 32807 |
| P646 | Freebase ID | /m/0dbp6y |
| P4317 | GARD rare disease ID | 6860 |
| P7464 | Genetics Home Reference Conditions ID | larsen-syndrome |
| P4229 | ICD-10-CM | Q74.8 |
| P665 | KEGG ID | H02048 |
| P486 | MeSH descriptor ID | C580241 |
| P6366 | Microsoft Academic ID (discontinued) | 2778272402 |
| P5270 | Mondo ID | MONDO_0007875 |
| P492 | OMIM ID | 150250 |
| P492 | OMIM ID | 150250 |
| P1550 | Orphanet ID | 503 |
| P2892 | UMLS CUI | C0175778 |
| P2892 | UMLS CUI | C1835564 |
| P2892 | UMLS CUI | C2931648 |
| P11430 | UniProt disease ID | DI-01214 |
| P11143 | WikiProjectMed ID | Larsen syndrome |
| P3471 | WikiSkripta article ID | 3103 |
Why not click here or view trends?
log id: 6109650