Wikidata entity: Q55783887
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2293 | genetic association | ... | Q14912231 (CD59) | CD59 |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P279 | subclass of | ... | Q55788287 (immunodeficiency due to a complement regulatory deficiency) | immunodeficiency due to a complement regulatory deficiency |
| P279 | subclass of | ... | Q55789123 (hereditary haemolytic anaemia due to red cell membrane defects) | hereditary haemolytic anaemia due to red cell membrane defects |
| P279 | subclass of | ... | Q55789138 (genetic peripheral neuropathy) | genetic peripheral neuropathy |
| P4229 | ICD-10-CM | D84.1 |
| P486 | MeSH descriptor ID | C567355 |
| P5270 | Mondo ID | MONDO_0012858 |
| P492 | OMIM ID | 612300 |
| P492 | OMIM ID | 612300 |
| P1550 | Orphanet ID | 169464 |
| P2892 | UMLS CUI | C2676767 |
| P11430 | UniProt disease ID | DI-01329 |
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log id: 5491675