As of 2022-03-07, the Wikidata property Patientplus ID (P1461) is used on 755 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 707
 0.0003
P646 Freebase ID 676
 0.0002
P486 MeSH descriptor ID 648
 0.0175
P10283 OpenAlex ID 617
 0.0061
P1995 health specialty 608
 0.0707
P672 MeSH tree code 605
 0.0364
P2892 UMLS CUI 590
 0.0237
P2888 exact match 573
 0.0002
P373 Commons category 573
 0.0002
P3827 JSTOR topic ID 551
 0.0217
P557 DiseasesDB 538
 0.1669
P7807 ICD-11 (foundation) 525
 0.0497
P673 eMedicine ID 505
 0.1755
P5008 on focus list of Wikimedia project 501
 0.0008
P604 MedlinePlus ID 485
 0.2154
P1417 Encyclopædia Britannica Online ID 481
 0.0028
P6366 Microsoft Academic ID 478
 0.0018
P699 Disease Ontology ID 468
 0.0431
P7329 ID (MMS) 465
 0.0567
P18 image 450
 0.0001
P1748 NCI Thesaurus ID 441
 0.0457
P31 instance of 435
 0.0000
P4229 ICD-10-CM 398
 0.0434
P5270 MonDO ID 393
 0.0219
P3417 Quora topic ID 379
 0.0021
P1692 ICD-9-CM 375
 0.0826
P508 BNCF Thesaurus ID 331
 0.0197
P244 Library of Congress authority ID 328
 0.0002
P5082 Store medisinske leksikon ID 309
 0.0909
P493 ICD-9 309
 0.0705
P3471 WikiSkripta ID 291
 0.1041
P494 ICD-10 284
 0.0565
P2176 drug or therapy used for treatment 283
 0.1599
P4317 GARD rare disease ID 279
 0.0503
P8189 National Library of Israel J9U ID 279
 0.0016
P665 KEGG ID 274
 0.0134
P8408 KBpedia ID 262
 0.0068
P3841 Human Phenotype Ontology ID 256
 0.1123
P7995 NHS Health A to Z ID 251
 0.2402
P1550 Orphanet ID 241
 0.0244
P2347 YSO ID 236
 0.0097
P1296 Gran Enciclopèdia Catalana ID 235
 0.0020
P667 ICPC 2 ID 231
 0.1578
P492 OMIM ID 231
 0.0093
P268 Bibliothèque nationale de France ID 228
 0.0004
P227 GND ID 213
 0.0002
P349 National Diet Library ID 196
 0.0014
P780 symptoms and signs 185
 0.0801
P910 topic's main category 185
 0.0003
P3219 Encyclopædia Universalis ID 182
 0.0054

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P7995 NHS Health A to Z ID 251
 0.2402
P604 MedlinePlus ID 485
 0.2154
P673 eMedicine ID 505
 0.1755
P557 DiseasesDB 538
 0.1669
P2176 drug or therapy used for treatment 283
 0.1599
P667 ICPC 2 ID 231
 0.1578
P3841 Human Phenotype Ontology ID 256
 0.1123
P3471 WikiSkripta ID 291
 0.1041
P5082 Store medisinske leksikon ID 309
 0.0909
P923 medical examinations 88
 0.0884
P1692 ICD-9-CM 375
 0.0826
P780 symptoms and signs 185
 0.0801
P7464 Genetics Home Reference Conditions ID 108
 0.0767
P924 possible treatment 72
 0.0727
P1995 health specialty 608
 0.0707
P493 ICD-9 309
 0.0705
P5806 SNOMED CT identifier 87
 0.0587
P7329 ID (MMS) 465
 0.0567
P494 ICD-10 284
 0.0565
P8656 Symptom Ontology ID 81
 0.0537
P1060 pathogen transmission process 47
 0.0516
P4317 GARD rare disease ID 279
 0.0503
P7807 ICD-11 (foundation) 525
 0.0497
P1748 NCI Thesaurus ID 441
 0.0457
P3487 maximal incubation period in humans 38
 0.0457
P3488 minimal incubation period in humans 38
 0.0456
P2074 internetmedicin.se ID 35
 0.0448
P4229 ICD-10-CM 398
 0.0434
P699 Disease Ontology ID 468
 0.0431
P1193 prevalence 33
 0.0407
P672 MeSH tree code 605
 0.0364
P668 GeneReviews ID 29
 0.0331
P6363 WordLift URL 72
 0.0321
P5642 risk factor 25
 0.0295
P1605 has natural reservoir 25
 0.0293
P9272 DeCS ID 62
 0.0257
P1550 Orphanet ID 241
 0.0244
P2892 UMLS CUI 590
 0.0237
P9084 ABC News topic ID 39
 0.0222
P5270 MonDO ID 393
 0.0219
P2004 NALT ID 157
 0.0218
P1583 MalaCards ID 17
 0.0217
P3827 JSTOR topic ID 551
 0.0217
P2293 genetic association 179
 0.0214
P4746 Elhuyar ZTH ID 145
 0.0202
P508 BNCF Thesaurus ID 331
 0.0197
P927 anatomical location 62
 0.0179
P3720 GPnotebook ID 21
 0.0178
P486 MeSH descriptor ID 648
 0.0175
P920 LEM ID 21
 0.0169