Wikidata entity: Q7578960
| P373 | Commons category | String | Spondyloepiphyseal dysplasia congenita | ??? |
| 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 | None | ??? |
| P2293 | genetic association | ... | Q14877681 (COL2A1) | COL2A1 |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P1692 | ICD-9-CM | String | 756.9 | ??? |
| P667 | ICPC 2 ID | String | L82 | ??? |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q7578956 (spondyloepiphyseal dysplasia) | spondyloepiphyseal dysplasia |
| P279 | subclass of | ... | Q18553439 (autosomal dominant disease) | autosomal dominant disease |
| P279 | subclass of | ... | Q18553493 (spondyloepiphyseal dysplasia with congenital joint dislocations) | spondyloepiphyseal dysplasia with congenital joint dislocations |
| P279 | subclass of | ... | Q18966185 (spondyloepimetaphyseal dysplasia) | spondyloepimetaphyseal dysplasia |
| P279 | subclass of | ... | Q55788797 (type 2 collagen-related bone disorder) | type 2 collagen-related bone disorder |
| P699 | Disease Ontology ID | DOID:14789 |
| P557 | DiseasesDB | 29410 |
| P673 | eMedicine ID | 1260836 |
| P4317 | GARD rare disease ID | 4987 |
| P668 | GeneReviews ID | NBK540447 |
| P7464 | Genetics Home Reference Conditions ID | spondyloepiphyseal-dysplasia-congenita |
| P3720 | GPnotebook ID | -1643773875 |
| P494 | ICD-10 ID | Q77.7 |
| P4229 | ICD-10-CM | Q77.7 |
| P493 | ICD-9 ID | 756.9 |
| P665 | KEGG ID | H00519 |
| P486 | MeSH descriptor ID | C535788 |
| P6366 | Microsoft Academic ID (discontinued) | 2779021635 |
| P5270 | Mondo ID | MONDO_0008471 |
| P492 | OMIM ID | 183900 |
| P492 | OMIM ID | 183900 |
| P1550 | Orphanet ID | 94068 |
| P2892 | UMLS CUI | C0038015 |
| P2892 | UMLS CUI | C2745959 |
| P11430 | UniProt disease ID | DI-02333 |
| P11143 | WikiProjectMed ID | Spondyloepiphyseal dysplasia congenita |
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