Wikidata entity: Q4162389
| 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 | ... | Q18031972 (TGFBI) | TGFBI |
| P1995 | health specialty | ... | Q161437 (ophthalmology) | ophthalmology |
| P1692 | ICD-9-CM | String | 371.52 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q929833 (rare disease) | rare 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 | ... | Q21154080 (epithelial and subepithelial dystrophy) | epithelial and subepithelial dystrophy |
| P279 | subclass of | ... | Q21154081 (epithelial-stromal TGFBI dystrophy) | epithelial-stromal TGFBI dystrophy |
| P699 | Disease Ontology ID | DOID:0060455 |
| P4317 | GARD rare disease ID | 9275 |
| P4229 | ICD-10-CM | H18.5 |
| P7807 | ICD-11 ID (Foundation) | 2082568100 |
| P665 | KEGG ID | H00952 |
| P486 | MeSH descriptor ID | C535942 |
| P5270 | Mondo ID | MONDO_0011185 |
| P492 | OMIM ID | 602082 |
| P492 | OMIM ID | 602082 |
| P1550 | Orphanet ID | 98960 |
| P2892 | UMLS CUI | C1562894 |
| P11430 | UniProt disease ID | DI-01429 |
| P11143 | WikiProjectMed ID | Thiel–Behnke dystrophy |
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