Wikidata entity: Q4147980
| P61 | discoverer or inventor | ... | Q4798912 (Arthur Groenouw) | Arthur Groenouw |
| 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 |
| 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 | ... | Q5596720 (corneal granular dystrophy) | corneal granular dystrophy |
| P279 | subclass of | ... | Q21154082 (stromal dystrophy) | stromal dystrophy |
| P699 | Disease Ontology ID | DOID:0080530 |
| P4317 | GARD rare disease ID | 9677 |
| P4229 | ICD-10-CM | H18.5 |
| P7807 | ICD-11 ID (Foundation) | 146332110 |
| P486 | MeSH descriptor ID | C537304 |
| P5270 | Mondo ID | MONDO_0007377 |
| P492 | OMIM ID | 121900 |
| P492 | OMIM ID | 121900 |
| P1550 | Orphanet ID | 98962 |
| P2892 | UMLS CUI | C1641846 |
| P11430 | UniProt disease ID | DI-01427 |
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log id: 5840360