Wikidata entity: Q492129
| P373 | Commons category | String | Porencephaly | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2888 | exact match | Url | None | ??? |
| P2888 | exact match | Url | None | ??? |
| P2888 | exact match | Url | Ontology Lookup Service (OLS) | ??? |
| P2293 | genetic association | ... | Q5145886 (COL4A1) | COL4A1 |
| P2293 | genetic association | ... | Q17907875 (COL4A2) | COL4A2 |
| P1995 | health specialty | ... | Q83042 (neurology) | neurology |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q576349 (encephalopathy) | encephalopathy |
| P279 | subclass of | ... | Q5062119 (central nervous system cyst) | central nervous system cyst |
| P279 | subclass of | ... | Q55003193 (malformations of cortical development, Group III) | malformations of cortical development, Group III |
| P9272 | DeCS ID | 55561 |
| P699 | Disease Ontology ID | DOID:0060263 |
| P557 | DiseasesDB | 33031 |
| P1417 | Encyclopædia Britannica Online ID | science/porencephaly |
| P646 | Freebase ID | /m/01hrc1 |
| P4317 | GARD rare disease ID | 7430 |
| P3841 | Human Phenotype Ontology ID | HP:0002132 |
| P4229 | ICD-10-CM | Q04.6 |
| P7807 | ICD-11 ID (Foundation) | 137059367 |
| P7329 | ICD-11 ID (MMS) | LA05.60 |
| P665 | KEGG ID | H00839 |
| P486 | MeSH descriptor ID | D065708 |
| P672 | MeSH tree code | C05.660.207.620.500 |
| P672 | MeSH tree code | C10.500.507.500.625 |
| P672 | MeSH tree code | C16.131.621.207.620.500 |
| P672 | MeSH tree code | C16.131.666.507.500.625 |
| P6366 | Microsoft Academic ID (discontinued) | 2778944715 |
| P5270 | Mondo ID | MONDO_0017410 |
| P492 | OMIM ID | 614483 |
| P492 | OMIM ID | 614483 |
| P10283 | OpenAlex ID | C2778944715 |
| P1550 | Orphanet ID | 2940 |
| P3417 | Quora topic ID | Porencephaly |
| P5806 | SNOMED CT ID | 38837006 |
| P2892 | UMLS CUI | C0302892 |
| P2892 | UMLS CUI | C1867983 |
| P2892 | UMLS CUI | C3698507 |
| P2892 | UMLS CUI | C4082173 |
| P11143 | WikiProjectMed ID | Porencephaly |
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