As of 2022-03-07, the Wikidata property prevalence (P1193) is used on 88 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 87
 0.0000
P1995 health specialty 84
 0.0099
P486 MeSH descriptor ID 79
 0.0021
P2888 exact match 79
 0.0000
P2892 UMLS CUI 78
 0.0032
P672 MeSH tree code 77
 0.0047
P646 Freebase ID 75
 0.0000
P5008 on focus list of Wikimedia project 74
 0.0001
P699 Disease Ontology ID 73
 0.0069
P557 DiseasesDB 72
 0.0238
P1748 NCI Thesaurus ID 69
 0.0074
P10283 OpenAlex ID 68
 0.0007
P7807 ICD-11 (foundation) 67
 0.0065
P4229 ICD-10-CM 66
 0.0075
P31 instance of 66
 0.0000
P673 eMedicine ID 64
 0.0241
P4317 GARD rare disease ID 63
 0.0124
P492 OMIM ID 63
 0.0026
P1550 Orphanet ID 59
 0.0063
P6366 Microsoft Academic ID 59
 0.0002
P2293 genetic association 56
 0.0072
P5270 MonDO ID 56
 0.0032
P7329 ID (MMS) 55
 0.0069
P373 Commons category 55
 0.0000
P604 MedlinePlus ID 53
 0.0263
P1417 Encyclopædia Britannica Online ID 53
 0.0003
P3827 JSTOR topic ID 52
 0.0021
P665 KEGG ID 51
 0.0025
P18 image 50
 0.0000
P1692 ICD-9-CM 46
 0.0110
P3417 Quora topic ID 44
 0.0002
P780 symptoms and signs 42
 0.0235
P244 Library of Congress authority ID 38
 0.0000
P828 has cause 36
 0.0047
P508 BNCF Thesaurus ID 36
 0.0022
P924 possible treatment 35
 0.0972
P923 medical examinations 34
 0.0888
P1461 Patientplus ID 33
 0.0407
P493 ICD-9 33
 0.0083
P8189 National Library of Israel J9U ID 33
 0.0002
P2176 drug or therapy used for treatment 31
 0.0229
P5082 Store medisinske leksikon ID 31
 0.0103
P494 ICD-10 31
 0.0067
P268 Bibliothèque nationale de France ID 30
 0.0001
P7995 NHS Health A to Z ID 29
 0.0483
P7464 Genetics Home Reference Conditions ID 28
 0.0341
P227 GND ID 28
 0.0000
P3471 WikiSkripta ID 27
 0.0113
P2347 YSO ID 25
 0.0010
P3841 Human Phenotype Ontology ID 24
 0.0130

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P924 possible treatment 35
 0.0972
P668 GeneReviews ID 21
 0.0963
P923 medical examinations 34
 0.0888
P7995 NHS Health A to Z ID 29
 0.0483
P1461 Patientplus ID 33
 0.0407
P7464 Genetics Home Reference Conditions ID 28
 0.0341
P8401 TheFreeDictionary medical term ID 3
 0.0316
P5085 Pschyrembel Online ID 3
 0.0273
P604 MedlinePlus ID 53
 0.0263
P5642 risk factor 5
 0.0249
P673 eMedicine ID 64
 0.0241
P557 DiseasesDB 72
 0.0238
P1199 mode of inheritance 4
 0.0238
P780 symptoms and signs 42
 0.0235
P1583 MalaCards ID 3
 0.0231
P2176 drug or therapy used for treatment 31
 0.0229
P2841 age of onset 2
 0.0217
P2074 internetmedicin.se ID 3
 0.0205
P2844 incidence 2
 0.0202
P2854 disease burden 2
 0.0200
P663 DSM-IV classification 2
 0.0196
P1930 DSM-5 classification 2
 0.0192
P667 ICPC 2 ID 19
 0.0188
P6532 has phenotype 3
 0.0163
P3487 maximal incubation period in humans 3
 0.0151
P3488 minimal incubation period in humans 3
 0.0149
P5806 SNOMED CT identifier 12
 0.0135
P5131 possible medical findings 2
 0.0134
P3841 Human Phenotype Ontology ID 24
 0.0130
P4317 GARD rare disease ID 63
 0.0124
P3471 WikiSkripta ID 27
 0.0113
P1692 ICD-9-CM 46
 0.0110
P653 PubMed Health 1
 0.0106
P8339 entry receptor 1
 0.0105
P5082 Store medisinske leksikon ID 31
 0.0103
P9186 DicoPolHiS ID 1
 0.0101
P1995 health specialty 84
 0.0099
P493 ICD-9 33
 0.0083
P4229 ICD-10-CM 66
 0.0075
P1748 NCI Thesaurus ID 69
 0.0074
P2293 genetic association 56
 0.0072
P1060 pathogen transmission process 2
 0.0069
P7329 ID (MMS) 55
 0.0069
P699 Disease Ontology ID 73
 0.0069
P5230 chromosome count 1
 0.0068
P494 ICD-10 31
 0.0067
P7807 ICD-11 (foundation) 67
 0.0065
P1550 Orphanet ID 59
 0.0063
P9084 ABC News topic ID 7
 0.0062
P10022 Dizionario di Medicina ID 1
 0.0060