As of 2022-03-07, the Wikidata property Disease Ontology ID (P699) is used on 10,574 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 10,570
0.0033
P279 subclass of 10,549
0.0040
P5008 on focus list of Wikimedia project 9,356
0.0141
P2892 UMLS CUI 8,586
0.3213
P5270 MonDO ID 8,112
0.4055
P1748 NCI Thesaurus ID 5,036
0.3387
P1995 health specialty 4,815
0.3388
P31 instance of 4,619
0.0000
P4229 ICD-10-CM 4,573
0.3087
P492 OMIM ID 4,251
0.1384
P486 MeSH descriptor ID 4,000
0.0919
P1550 Orphanet ID 3,191
0.1903
P1692 ICD-9-CM 3,031
0.2590
P2293 genetic association 3,000
0.1954
P7807 ICD-11 (foundation) 2,962
0.1651
P6366 Microsoft Academic ID 2,632
0.0095
P4317 GARD rare disease ID 2,590
0.1983
P672 MeSH tree code 2,455
0.0999
P7329 ID (MMS) 2,111
0.1289
P646 Freebase ID 1,894
0.0004
P557 DiseasesDB 1,837
0.1564
P10283 OpenAlex ID 1,752
0.0161
P373 Commons category 1,607
0.0005
P665 KEGG ID 1,584
0.0547
P673 eMedicine ID 1,350
0.1139
P3827 JSTOR topic ID 1,349
0.0392
P1417 Encyclopædia Britannica Online ID 1,159
0.0064
P494 ICD-10 1,107
0.0789
P927 anatomical location 1,066
0.0868
P493 ICD-9 1,023
0.0758
P604 MedlinePlus ID 997
0.0863
P18 image 987
0.0002
P2176 drug or therapy used for treatment 972
0.0892
P3841 Human Phenotype Ontology ID 890
0.0776
P780 symptoms and signs 770
0.0667
P3417 Quora topic ID 727
0.0038
P7464 Genetics Home Reference Conditions ID 611
0.0570
P244 Library of Congress authority ID 575
0.0004
P508 BNCF Thesaurus ID 572
0.0217
P5082 Store medisinske leksikon ID 555
0.0428
P563 ICD-O 547
0.0499
P828 has cause 522
0.0297
P2581 BabelNet ID 519
0.0063
P667 ICPC 2 ID 483
0.0438
P1461 Patientplus ID 468
0.0431
P910 topic's main category 468
0.0007
P8408 KBpedia ID 457
0.0095
P1296 Gran Enciclopèdia Catalana ID 438
0.0035
P3471 WikiSkripta ID 428
0.0343
P5806 SNOMED CT identifier 424
0.0387

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P5270 MonDO ID 8,112
0.4055
P1995 health specialty 4,815
0.3388
P1748 NCI Thesaurus ID 5,036
0.3387
P2892 UMLS CUI 8,586
0.3213
P4229 ICD-10-CM 4,573
0.3087
P1692 ICD-9-CM 3,031
0.2590
P4317 GARD rare disease ID 2,590
0.1983
P2293 genetic association 3,000
0.1954
P1550 Orphanet ID 3,191
0.1903
P7807 ICD-11 (foundation) 2,962
0.1651
P557 DiseasesDB 1,837
0.1564
P492 OMIM ID 4,251
0.1384
P7329 ID (MMS) 2,111
0.1289
P673 eMedicine ID 1,350
0.1139
P672 MeSH tree code 2,455
0.0999
P486 MeSH descriptor ID 4,000
0.0919
P2176 drug or therapy used for treatment 972
0.0892
P927 anatomical location 1,066
0.0868
P604 MedlinePlus ID 997
0.0863
P494 ICD-10 1,107
0.0789
P3841 Human Phenotype Ontology ID 890
0.0776
P493 ICD-9 1,023
0.0758
P780 symptoms and signs 770
0.0667
P7464 Genetics Home Reference Conditions ID 611
0.0570
P665 KEGG ID 1,584
0.0547
P563 ICD-O 547
0.0499
P667 ICPC 2 ID 483
0.0438
P1461 Patientplus ID 468
0.0431
P5082 Store medisinske leksikon ID 555
0.0428
P3827 JSTOR topic ID 1,349
0.0392
P5806 SNOMED CT identifier 424
0.0387
P7995 NHS Health A to Z ID 371
0.0345
P3471 WikiSkripta ID 428
0.0343
P828 has cause 522
0.0297
P508 BNCF Thesaurus ID 572
0.0217
P923 medical examinations 208
0.0194
P689 afflicts 198
0.0169
P924 possible treatment 179
0.0167
P4746 Elhuyar ZTH ID 273
0.0162
P10283 OpenAlex ID 1,752
0.0161
P5008 on focus list of Wikimedia project 9,356
0.0141
P2004 NALT ID 239
0.0141
P1060 pathogen transmission process 141
0.0133
P668 GeneReviews ID 134
0.0127
P2347 YSO ID 398
0.0117
P1245 OmegaWiki Defined Meaning 247
0.0113
P9272 DeCS ID 124
0.0102
P6366 Microsoft Academic ID 2,632
0.0095
P8408 KBpedia ID 457
0.0095
P3488 minimal incubation period in humans 98
0.0093