Wikidata entity: Q18767
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P1995 | health specialty | ... | Q83042 (neurology) | neurology |
| P667 | ICPC 2 ID | String | N99 | ??? |
| P31 | instance of | ... | Q1441305 (clinical sign) | clinical sign |
| P31 | instance of | ... | Q3339235 (neurological disorder) | neurological disorder |
| P31 | instance of | ... | Q112965645 (symptom or sign) | symptom or sign |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P1748 | NCI Thesaurus ID | String | C85024 | ??? |
| P279 | subclass of | ... | Q2836 (aphasia) | aphasia |
| P279 | subclass of | ... | Q1755684 (corticobasal degeneration) | corticobasal degeneration |
| P279 | subclass of | ... | Q55346096 (neurodegenerative disease with dementia) | neurodegenerative disease with dementia |
| P2581 | BabelNet ID | 01887937n |
| P2581 | BabelNet ID | 01887937n |
| P11956 | Experimental Factor Ontology ID | 0009053 |
| P646 | Freebase ID | /m/07lx94 |
| P4317 | GARD rare disease ID | 8541 |
| P4229 | ICD-10-CM | G31.0 |
| P486 | MeSH descriptor ID | D018888 |
| P672 | MeSH tree code | C10.228.140.380.132 |
| P672 | MeSH tree code | C10.597.606.150.500.800.100.155 |
| P672 | MeSH tree code | C23.888.592.604.150.500.800.100.155 |
| P672 | MeSH tree code | F03.615.400.125 |
| P5270 | Mondo ID | MONDO_0019806 |
| P492 | OMIM ID | 607485 |
| P492 | OMIM ID | 607485 |
| P10283 | OpenAlex ID | C2779140760 |
| P1550 | Orphanet ID | 95432 |
| P4233 | PatientsLikeMe condition ID | primary-progressive-aphasia |
| P2892 | UMLS CUI | C0282513 |
| P11143 | WikiProjectMed ID | Primary progressive aphasia |
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