As of 2022-03-07, the Wikidata property Human Phenotype Ontology ID (P3841) is used on 1,781 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
P2892 UMLS CUI 1,639
 0.0659
P279 subclass of 1,638
 0.0006
P2888 exact match 1,601
 0.0005
P486 MeSH descriptor ID 1,402
 0.0376
P1995 health specialty 1,270
 0.1417
P672 MeSH tree code 1,153
 0.0675
P5270 MonDO ID 1,076
 0.0590
P7807 ICD-11 (foundation) 990
 0.0890
P6366 Microsoft Academic ID 986
 0.0036
P10283 OpenAlex ID 983
 0.0097
P646 Freebase ID 948
 0.0002
P5008 on focus list of Wikimedia project 942
 0.0014
P31 instance of 922
 0.0000
P699 Disease Ontology ID 890
 0.0776
P1748 NCI Thesaurus ID 862
 0.0841
P373 Commons category 832
 0.0002
P7329 ID (MMS) 812
 0.0914
P557 DiseasesDB 800
 0.2006
P4229 ICD-10-CM 785
 0.0800
P3827 JSTOR topic ID 779
 0.0297
P493 ICD-9 658
 0.1300
P1692 ICD-9-CM 643
 0.1214
P494 ICD-10 632
 0.1108
P673 eMedicine ID 606
 0.1594
P1417 Encyclopædia Britannica Online ID 594
 0.0034
P604 MedlinePlus ID 560
 0.1748
P492 OMIM ID 540
 0.0211
P1550 Orphanet ID 537
 0.0505
P18 image 497
 0.0001
P4317 GARD rare disease ID 473
 0.0741
P3417 Quora topic ID 439
 0.0024
P5082 Store medisinske leksikon ID 399
 0.0920
P508 BNCF Thesaurus ID 396
 0.0223
P2176 drug or therapy used for treatment 391
 0.1455
P244 Library of Congress authority ID 367
 0.0003
P667 ICPC 2 ID 325
 0.1356
P2293 genetic association 321
 0.0347
P665 KEGG ID 307
 0.0143
P1296 Gran Enciclopèdia Catalana ID 285
 0.0025
P3471 WikiSkripta ID 267
 0.0694
P8189 National Library of Israel J9U ID 263
 0.0015
P268 Bibliothèque nationale de France ID 258
 0.0004
P1461 Patientplus ID 256
 0.1123
P2347 YSO ID 227
 0.0090
P4746 Elhuyar ZTH ID 226
 0.0278
P8408 KBpedia ID 225
 0.0057
P1343 described by source 223
 0.0003
P227 GND ID 220
 0.0002
P2581 BabelNet ID 213
 0.0029
P910 topic's main category 209
 0.0003

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P557 DiseasesDB 800
 0.2006
P604 MedlinePlus ID 560
 0.1748
P673 eMedicine ID 606
 0.1594
P2176 drug or therapy used for treatment 391
 0.1455
P1995 health specialty 1,270
 0.1417
P667 ICPC 2 ID 325
 0.1356
P493 ICD-9 658
 0.1300
P1692 ICD-9-CM 643
 0.1214
P1461 Patientplus ID 256
 0.1123
P494 ICD-10 632
 0.1108
P5082 Store medisinske leksikon ID 399
 0.0920
P7329 ID (MMS) 812
 0.0914
P7995 NHS Health A to Z ID 192
 0.0901
P7807 ICD-11 (foundation) 990
 0.0890
P1748 NCI Thesaurus ID 862
 0.0841
P4229 ICD-10-CM 785
 0.0800
P699 Disease Ontology ID 890
 0.0776
P8656 Symptom Ontology ID 183
 0.0752
P5806 SNOMED CT identifier 180
 0.0746
P4317 GARD rare disease ID 473
 0.0741
P3471 WikiSkripta ID 267
 0.0694
P672 MeSH tree code 1,153
 0.0675
P2892 UMLS CUI 1,639
 0.0659
P5270 MonDO ID 1,076
 0.0590
P1550 Orphanet ID 537
 0.0505
P7464 Genetics Home Reference Conditions ID 121
 0.0500
P780 symptoms and signs 143
 0.0423
P563 ICD-O 102
 0.0389
P486 MeSH descriptor ID 1,402
 0.0376
P2293 genetic association 321
 0.0347
P927 anatomical location 142
 0.0322
P3827 JSTOR topic ID 779
 0.0297
P689 afflicts 85
 0.0282
P4746 Elhuyar ZTH ID 226
 0.0278
P924 possible treatment 52
 0.0255
P508 BNCF Thesaurus ID 396
 0.0223
P492 OMIM ID 540
 0.0211
P9272 DeCS ID 72
 0.0210
P2074 internetmedicin.se ID 37
 0.0205
P923 medical examinations 41
 0.0198
P6363 WordLift URL 64
 0.0195
P2004 NALT ID 154
 0.0187
P3720 GPnotebook ID 37
 0.0169
P5131 possible medical findings 27
 0.0149
P668 GeneReviews ID 28
 0.0147
P665 KEGG ID 307
 0.0143
P8061 AGROVOC ID 47
 0.0137
P1193 prevalence 24
 0.0130
P5642 risk factor 23
 0.0123
P1245 OmegaWiki Defined Meaning 159
 0.0121