As of 2022-03-07, the Wikidata property Genetics Home Reference Conditions ID (P7464) is used on 762 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 757
 0.0003
P2888 exact match 715
 0.0002
P2892 UMLS CUI 678
 0.0273
P1550 Orphanet ID 669
 0.0706
P492 OMIM ID 660
 0.0269
P4317 GARD rare disease ID 650
 0.1253
P31 instance of 617
 0.0000
P699 Disease Ontology ID 611
 0.0570
P486 MeSH descriptor ID 601
 0.0162
P4229 ICD-10-CM 586
 0.0652
P5008 on focus list of Wikimedia project 577
 0.0009
P2293 genetic association 573
 0.0719
P665 KEGG ID 559
 0.0277
P5270 MonDO ID 558
 0.0314
P6366 Microsoft Academic ID 516
 0.0019
P1995 health specialty 499
 0.0573
P1748 NCI Thesaurus ID 481
 0.0501
P557 DiseasesDB 468
 0.1418
P7807 ICD-11 (foundation) 392
 0.0366
P646 Freebase ID 364
 0.0001
P672 MeSH tree code 334
 0.0198
P1692 ICD-9-CM 297
 0.0642
P673 eMedicine ID 271
 0.0869
P373 Commons category 265
 0.0001
P10283 OpenAlex ID 259
 0.0026
P7329 ID (MMS) 233
 0.0276
P493 ICD-9 220
 0.0491
P3827 JSTOR topic ID 189
 0.0073
P1417 Encyclopædia Britannica Online ID 179
 0.0010
P604 MedlinePlus ID 176
 0.0685
P494 ICD-10 165
 0.0320
P18 image 161
 0.0000
P3417 Quora topic ID 130
 0.0007
P3841 Human Phenotype Ontology ID 121
 0.0500
P780 symptoms and signs 117
 0.0491
P138 named after 117
 0.0003
P1461 Patientplus ID 108
 0.0767
P1325 external data available at 107
 0.0053
P2176 drug or therapy used for treatment 97
 0.0494
P668 GeneReviews ID 92
 0.1121
P3471 WikiSkripta ID 89
 0.0296
P244 Library of Congress authority ID 87
 0.0001
P7995 NHS Health A to Z ID 83
 0.0680
P2347 YSO ID 82
 0.0034
P5806 SNOMED CT identifier 79
 0.0528
P8189 National Library of Israel J9U ID 76
 0.0004
P508 BNCF Thesaurus ID 74
 0.0043
P2581 BabelNet ID 74
 0.0010
P8408 KBpedia ID 71
 0.0018
P667 ICPC 2 ID 68
 0.0416

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P557 DiseasesDB 468
 0.1418
P4317 GARD rare disease ID 650
 0.1253
P668 GeneReviews ID 92
 0.1121
P673 eMedicine ID 271
 0.0869
P1461 Patientplus ID 108
 0.0767
P2293 genetic association 573
 0.0719
P1550 Orphanet ID 669
 0.0706
P604 MedlinePlus ID 176
 0.0685
P7995 NHS Health A to Z ID 83
 0.0680
P4229 ICD-10-CM 586
 0.0652
P1692 ICD-9-CM 297
 0.0642
P1995 health specialty 499
 0.0573
P699 Disease Ontology ID 611
 0.0570
P5806 SNOMED CT identifier 79
 0.0528
P1748 NCI Thesaurus ID 481
 0.0501
P3841 Human Phenotype Ontology ID 121
 0.0500
P2176 drug or therapy used for treatment 97
 0.0494
P493 ICD-9 220
 0.0491
P780 symptoms and signs 117
 0.0491
P667 ICPC 2 ID 68
 0.0416
P7807 ICD-11 (foundation) 392
 0.0366
P1193 prevalence 28
 0.0341
P494 ICD-10 165
 0.0320
P5270 MonDO ID 558
 0.0314
P3471 WikiSkripta ID 89
 0.0296
P665 KEGG ID 559
 0.0277
P7329 ID (MMS) 233
 0.0276
P2892 UMLS CUI 678
 0.0273
P492 OMIM ID 660
 0.0269
P923 medical examinations 27
 0.0254
P1199 mode of inheritance 18
 0.0217
P924 possible treatment 22
 0.0210
P6532 has phenotype 17
 0.0201
P672 MeSH tree code 334
 0.0198
P5082 Store medisinske leksikon ID 65
 0.0178
P9272 DeCS ID 41
 0.0168
P486 MeSH descriptor ID 601
 0.0162
P563 ICD-O 25
 0.0149
P1583 MalaCards ID 8
 0.0100
P2074 internetmedicin.se ID 8
 0.0098
P5642 risk factor 7
 0.0080
P3827 JSTOR topic ID 189
 0.0073
P689 afflicts 14
 0.0068
P1325 external data available at 107
 0.0053
P9084 ABC News topic ID 9
 0.0050
P3720 GPnotebook ID 6
 0.0050
P5131 possible medical findings 4
 0.0049
P2004 NALT ID 33
 0.0045
P508 BNCF Thesaurus ID 74
 0.0043
P927 anatomical location 15
 0.0043