As of 2022-03-07, the Wikidata property ICD-10-CM (P4229) is used on 8,811 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
P2888 exact match 8,521
0.0026
P279 subclass of 8,514
0.0032
P5270 MonDO ID 8,069
0.4412
P2892 UMLS CUI 6,679
0.2486
P1550 Orphanet ID 6,301
0.5299
P31 instance of 5,122
0.0001
P699 Disease Ontology ID 4,573
0.3087
P5008 on focus list of Wikimedia project 4,480
0.0067
P486 MeSH descriptor ID 3,911
0.0934
P1995 health specialty 3,793
0.2816
P492 OMIM ID 3,723
0.1262
P7807 ICD-11 (foundation) 3,175
0.1989
P4317 GARD rare disease ID 2,957
0.2706
P1692 ICD-9-CM 2,764
0.2708
P1748 NCI Thesaurus ID 2,650
0.1711
P2293 genetic association 2,511
0.1784
P6366 Microsoft Academic ID 2,366
0.0086
P7329 ID (MMS) 2,141
0.1468
P672 MeSH tree code 1,778
0.0757
P557 DiseasesDB 1,654
0.1627
P646 Freebase ID 1,643
0.0004
P665 KEGG ID 1,555
0.0571
P10283 OpenAlex ID 1,406
0.0131
P373 Commons category 1,360
0.0004
P673 eMedicine ID 1,177
0.1147
P3827 JSTOR topic ID 1,052
0.0319
P1417 Encyclopædia Britannica Online ID 994
0.0055
P493 ICD-9 907
0.0766
P494 ICD-10 889
0.0712
P604 MedlinePlus ID 863
0.0869
P18 image 856
0.0002
P3841 Human Phenotype Ontology ID 785
0.0800
P2176 drug or therapy used for treatment 758
0.0811
P780 symptoms and signs 632
0.0637
P3417 Quora topic ID 621
0.0032
P7464 Genetics Home Reference Conditions ID 586
0.0652
P508 BNCF Thesaurus ID 485
0.0197
P244 Library of Congress authority ID 480
0.0004
P5082 Store medisinske leksikon ID 461
0.0408
P927 anatomical location 456
0.0410
P828 has cause 426
0.0267
P667 ICPC 2 ID 415
0.0445
P1461 Patientplus ID 398
0.0434
P8408 KBpedia ID 395
0.0085
P2581 BabelNet ID 387
0.0048
P2671 Google Knowledge Graph ID 377
0.0001
P3471 WikiSkripta ID 374
0.0347
P1296 Gran Enciclopèdia Catalana ID 352
0.0029
P910 topic's main category 346
0.0005
P5806 SNOMED CT identifier 339
0.0365

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P1550 Orphanet ID 6,301
0.5299
P5270 MonDO ID 8,069
0.4412
P699 Disease Ontology ID 4,573
0.3087
P1995 health specialty 3,793
0.2816
P1692 ICD-9-CM 2,764
0.2708
P4317 GARD rare disease ID 2,957
0.2706
P2892 UMLS CUI 6,679
0.2486
P7807 ICD-11 (foundation) 3,175
0.1989
P2293 genetic association 2,511
0.1784
P1748 NCI Thesaurus ID 2,650
0.1711
P557 DiseasesDB 1,654
0.1627
P7329 ID (MMS) 2,141
0.1468
P492 OMIM ID 3,723
0.1262
P673 eMedicine ID 1,177
0.1147
P486 MeSH descriptor ID 3,911
0.0934
P604 MedlinePlus ID 863
0.0869
P2176 drug or therapy used for treatment 758
0.0811
P3841 Human Phenotype Ontology ID 785
0.0800
P493 ICD-9 907
0.0766
P672 MeSH tree code 1,778
0.0757
P494 ICD-10 889
0.0712
P7464 Genetics Home Reference Conditions ID 586
0.0652
P780 symptoms and signs 632
0.0637
P665 KEGG ID 1,555
0.0571
P667 ICPC 2 ID 415
0.0445
P1461 Patientplus ID 398
0.0434
P927 anatomical location 456
0.0410
P5082 Store medisinske leksikon ID 461
0.0408
P5806 SNOMED CT identifier 339
0.0365
P3471 WikiSkripta ID 374
0.0347
P7995 NHS Health A to Z ID 313
0.0346
P3827 JSTOR topic ID 1,052
0.0319
P828 has cause 426
0.0267
P563 ICD-O 226
0.0237
P923 medical examinations 196
0.0219
P508 BNCF Thesaurus ID 485
0.0197
P924 possible treatment 164
0.0183
P4746 Elhuyar ZTH ID 228
0.0150
P689 afflicts 139
0.0139
P1060 pathogen transmission process 123
0.0138
P668 GeneReviews ID 116
0.0131
P2004 NALT ID 199
0.0131
P10283 OpenAlex ID 1,406
0.0131
P3488 minimal incubation period in humans 95
0.0108
P3487 maximal incubation period in humans 93
0.0105
P9272 DeCS ID 107
0.0103
P1245 OmegaWiki Defined Meaning 206
0.0102
P2347 YSO ID 330
0.0102
P8656 Symptom Ontology ID 87
0.0091
P6366 Microsoft Academic ID 2,366
0.0086