Wikidata entity: Q371520
| P373 | Commons category | String | Polydactyly | ??? |
| P1343 | described by source | ... | Q19219752 (Meyers Konversations-Lexikon, 4th edition (1885–1890)) | Meyers Konversations-Lexikon, 4th edition (1885–1890) |
| P1343 | described by source | ... | Q20078554 (Great Soviet Encyclopedia (1926–1947)) | Great Soviet Encyclopedia (1926–1947) |
| 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) | ??? |
| P2293 | genetic association | ... | Q14886904 (GLI3) | GLI3 |
| P2293 | genetic association | ... | Q18045636 (LMBR1) | LMBR1 |
| P1995 | health specialty | ... | Q1071953 (medical genetics) | medical genetics |
| P1692 | ICD-9-CM | String | 755.0 | ??? |
| P1692 | ICD-9-CM | String | 755.00 | ??? |
| P667 | ICPC 2 ID | String | L82 | ??? |
| P31 | instance of | ... | Q929833 (rare disease) | rare disease |
| P31 | instance of | ... | Q112193867 (class of disease) | class of disease |
| P31 | instance of | ... | Q55788864 (developmental defect during embryogenesis) | developmental defect during embryogenesis |
| P1748 | NCI Thesaurus ID | String | C87110 | ??? |
| P5008 | on focus list of Wikimedia project | ... | Q4099686 (WikiProject Medicine) | WikiProject Medicine |
| P279 | subclass of | ... | Q12136 (disease) | disease |
| P279 | subclass of | ... | Q727096 (congenital disorder) | congenital disorder |
| P279 | subclass of | ... | Q61642689 (congenital anomaly of digit) | congenital anomaly of digit |
| P279 | subclass of | ... | Q5160441 (congenital limb deformity) | congenital limb deformity |
| P279 | subclass of | ... | Q55788826 (non-syndromic polydactyly, syndactyly and/or hyperphalangy) | non-syndromic polydactyly, syndactyly and/or hyperphalangy |
| P699 | Disease Ontology ID | DOID:1148 |
| P557 | DiseasesDB | 24853 |
| P673 | eMedicine ID | 1113584 |
| P1417 | Encyclopædia Britannica Online ID | science/polydactyly |
| P646 | Freebase ID | /m/01bb3r |
| P4317 | GARD rare disease ID | 4410 |
| P2924 | Great Russian Encyclopedia Online ID (old version) | 3153167 |
| P3841 | Human Phenotype Ontology ID | HP:0010442 |
| P4229 | ICD-10-CM | Q69 |
| P4229 | ICD-10-CM | Q69.2 |
| P4229 | ICD-10-CM | Q69.0 |
| P4229 | ICD-10-CM | Q69.1 |
| P4229 | ICD-10-CM | Q69.9 |
| P7807 | ICD-11 ID (Foundation) | 1534380955 |
| P7329 | ICD-11 ID (MMS) | LB78 |
| P3827 | JSTOR topic ID (archived) | polydactyly |
| P665 | KEGG ID | H02332 |
| P604 | MedlinePlus ID | 003176 |
| P604 | MedlinePlus ID | 003176 |
| P486 | MeSH descriptor ID | D017689 |
| P672 | MeSH tree code | C05.660.585.600 |
| P672 | MeSH tree code | C16.131.621.585.600 |
| P6366 | Microsoft Academic ID (discontinued) | 2777267824 |
| P6366 | Microsoft Academic ID (discontinued) | 2910325542 |
| P6366 | Microsoft Academic ID (discontinued) | 2910421294 |
| P5270 | Mondo ID | MONDO_0011348 |
| P8885 | Namuwiki ID | 다지증 |
| P1245 | OmegaWiki Defined Meaning | 1100436 |
| P492 | OMIM ID | 174200 |
| P492 | OMIM ID | 174200 |
| P492 | OMIM ID | 174700 |
| P492 | OMIM ID | 174700 |
| P492 | OMIM ID | 174500 |
| P492 | OMIM ID | 174500 |
| P492 | OMIM ID | 603596 |
| P492 | OMIM ID | 603596 |
| P10283 | OpenAlex ID | C2777267824 |
| P1550 | Orphanet ID | 2913 |
| P3417 | Quora topic ID | Polydactyly |
| P5806 | SNOMED CT ID | 367506006 |
| P5082 | Store medisinske leksikon ID | polydaktyli |
| P2892 | UMLS CUI | C0152427 |
| P11143 | WikiProjectMed ID | Polydactyly |
| P3471 | WikiSkripta article ID | 25968 |
| P8814 | WordNet 3.1 Synset ID | 14495308-n |
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