As of 2022-03-07, the Wikidata property ICD-11 (foundation) (P7807) is used on 10,328 items as main value on statements (not counting qualifiers) of the Q and P namespaces.

Closest properties: by cardinality of intersection, by Jaccard index.

Display properties of the following types:                                    

Closest properties by cardinality of intersection

IDLabelIntersection cardinalityJaccard index
P279 subclass of 9,302
0.0035
P7329 ID (MMS) 7,903
0.7644
P2892 UMLS CUI 5,791
0.1979
P6366 Microsoft Academic ID 5,156
0.0187
P31 instance of 5,131
0.0001
P2888 exact match 4,602
0.0014
P486 MeSH descriptor ID 4,323
0.1006
P646 Freebase ID 4,085
0.0009
P5270 MonDO ID 3,995
0.1673
P1995 health specialty 3,853
0.2581
P5008 on focus list of Wikimedia project 3,499
0.0052
P10283 OpenAlex ID 3,191
0.0297
P672 MeSH tree code 3,182
0.1348
P4229 ICD-10-CM 3,175
0.1989
P373 Commons category 3,127
0.0009
P699 Disease Ontology ID 2,962
0.1651
P1748 NCI Thesaurus ID 2,837
0.1687
P1550 Orphanet ID 2,617
0.1531
P494 ICD-10 2,495
0.2014
P18 image 2,295
0.0006
P3827 JSTOR topic ID 2,173
0.0651
P1692 ICD-9-CM 2,152
0.1745
P1417 Encyclopædia Britannica Online ID 2,135
0.0119
P1402 Foundational Model of Anatomy ID 2,029
0.0232
P557 DiseasesDB 1,905
0.1667
P493 ICD-9 1,889
0.1526
P4317 GARD rare disease ID 1,788
0.1313
P1343 described by source 1,765
0.0025
P673 eMedicine ID 1,532
0.1341
P492 OMIM ID 1,468
0.0441
P7173 TA2 ID 1,395
0.1092
P1323 Terminologia Anatomica 98 ID 1,391
0.1083
P3982 TA98 Latin term 1,381
0.1076
P8408 KBpedia ID 1,349
0.0286
P3417 Quora topic ID 1,275
0.0066
P604 MedlinePlus ID 1,168
0.1048
P665 KEGG ID 1,164
0.0400
P508 BNCF Thesaurus ID 1,141
0.0447
P1554 UBERON ID 1,128
0.0925
P244 Library of Congress authority ID 1,117
0.0008
P910 topic's main category 1,090
0.0016
P3841 Human Phenotype Ontology ID 990
0.0890
P2293 genetic association 930
0.0541
P5082 Store medisinske leksikon ID 918
0.0742
P3471 WikiSkripta ID 884
0.0751
P2176 drug or therapy used for treatment 843
0.0782
P227 GND ID 823
0.0006
P268 Bibliothèque nationale de France ID 808
0.0014
P1296 Gran Enciclopèdia Catalana ID 791
0.0064
P171 parent taxon 789
0.0002

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P7329 ID (MMS) 7,903
0.7644
P1995 health specialty 3,853
0.2581
P494 ICD-10 2,495
0.2014
P4229 ICD-10-CM 3,175
0.1989
P2892 UMLS CUI 5,791
0.1979
P1692 ICD-9-CM 2,152
0.1745
P1748 NCI Thesaurus ID 2,837
0.1687
P5270 MonDO ID 3,995
0.1673
P557 DiseasesDB 1,905
0.1667
P699 Disease Ontology ID 2,962
0.1651
P1550 Orphanet ID 2,617
0.1531
P493 ICD-9 1,889
0.1526
P672 MeSH tree code 3,182
0.1348
P673 eMedicine ID 1,532
0.1341
P4317 GARD rare disease ID 1,788
0.1313
P7173 TA2 ID 1,395
0.1092
P1323 Terminologia Anatomica 98 ID 1,391
0.1083
P3982 TA98 Latin term 1,381
0.1076
P604 MedlinePlus ID 1,168
0.1048
P486 MeSH descriptor ID 4,323
0.1006
P1554 UBERON ID 1,128
0.0925
P3841 Human Phenotype Ontology ID 990
0.0890
P2176 drug or therapy used for treatment 843
0.0782
P3471 WikiSkripta ID 884
0.0751
P5082 Store medisinske leksikon ID 918
0.0742
P3827 JSTOR topic ID 2,173
0.0651
P667 ICPC 2 ID 651
0.0613
P563 ICD-O 610
0.0572
P2293 genetic association 930
0.0541
P780 symptoms and signs 610
0.0532
P927 anatomical location 655
0.0526
P1461 Patientplus ID 525
0.0497
P5806 SNOMED CT identifier 499
0.0469
P508 BNCF Thesaurus ID 1,141
0.0447
P492 OMIM ID 1,468
0.0441
P665 KEGG ID 1,164
0.0400
P7995 NHS Health A to Z ID 402
0.0384
P7464 Genetics Home Reference Conditions ID 392
0.0366
P828 has cause 598
0.0346
P2004 NALT ID 562
0.0344
P4746 Elhuyar ZTH ID 513
0.0313
P10283 OpenAlex ID 3,191
0.0297
P8408 KBpedia ID 1,349
0.0286
P8656 Symptom Ontology ID 300
0.0276
P1245 OmegaWiki Defined Meaning 553
0.0260
P3720 GPnotebook ID 259
0.0246
P1402 Foundational Model of Anatomy ID 2,029
0.0232
P923 medical examinations 224
0.0215
P1542 has effect 292
0.0208
P2347 YSO ID 672
0.0201