Wikidata entity: Q899726
| 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 | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P1325 | external data available at URL | Url | None | ??? |
| P1995 | health specialty | ... | Q83042 (neurology) | neurology |
| P1692 | ICD-9-CM | String | 334.3 | ??? |
| P667 | ICPC 2 ID | String | N99 | ??? |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q112965645 (symptom or sign) | symptom or sign |
| P31 | instance of | ... | Q42303753 (designated intractable/rare disease) | designated intractable/rare disease |
| P1748 | NCI Thesaurus ID | String | C82341 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| 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 | ... | Q66124188 (spinocerebellar degenerations) | spinocerebellar degenerations |
| P279 | subclass of | ... | Q18553439 (autosomal dominant disease) | autosomal dominant 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 | ... | Q55346100 (late-onset ataxia with dementia) | late-onset ataxia with dementia |
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log id: 9425128