Wikidata entity: Q4826996
| 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) | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q154709 (cerebellar ataxia) | cerebellar ataxia |
| P279 | subclass of | ... | Q1620193 (cerebral degeneration) | cerebral degeneration |
| P279 | subclass of | ... | Q3731293 (hereditary ataxia) | hereditary ataxia |
| P279 | subclass of | ... | Q10267817 (autosomal recessive disease) | autosomal recessive disease |
| P279 | subclass of | ... | Q18558225 (eye degenerative disease) | eye degenerative disease |
| P279 | subclass of | ... | Q19001236 (nervous system heredodegenerative disease) | nervous system heredodegenerative disease |
| P279 | subclass of | ... | Q55346099 (early-onset ataxia with dementia) | early-onset ataxia with dementia |
| P279 | subclass of | ... | Q55785843 (genetic movement disorder) | genetic movement disorder |
| P279 | subclass of | ... | Q55785846 (rare genetic developmental defect during embryogenesis) | rare genetic developmental defect during embryogenesis |
| P279 | subclass of | ... | Q55789257 (spinocerebellar ataxia with oculomotor anomaly) | spinocerebellar ataxia with oculomotor anomaly |
| P699 | Disease Ontology ID | DOID:0050950 |
| P665 | KEGG ID | H01891 |
| P5270 | Mondo ID | MONDO_0015244 |
| P492 | OMIM ID | 610743 |
| P492 | OMIM ID | 610743 |
| P1550 | Orphanet ID | 1172 |
| P2892 | UMLS CUI | C5575375 |
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