As of 2022-03-07, the Wikidata property genetic association (P2293) is used on 7,778 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 7,584
 0.0029
P492 OMIM ID 7,355
 0.2963
P2888 exact match 7,327
 0.0023
P31 instance of 7,307
 0.0001
P2892 UMLS CUI 3,790
 0.1320
P5270 MonDO ID 3,572
 0.1642
P703 found in taxon 3,539
 0.0014
P351 Entrez Gene ID 3,535
 0.0045
P353 HGNC gene symbol 3,528
 0.0736
P354 HGNC ID 3,527
 0.0738
P594 Ensembl gene ID 3,521
 0.0227
P639 RefSeq RNA ID 3,518
 0.0130
P688 encodes 3,502
 0.0036
P593 HomoloGene ID 3,491
 0.0334
P4196 cytogenetic location 3,482
 0.0183
P1057 chromosome 3,472
 0.0057
P644 genomic start 3,470
 0.0034
P645 genomic end 3,470
 0.0034
P704 Ensembl transcript ID 3,469
 0.0248
P2548 strand orientation 3,468
 0.0034
P5572 expressed in 3,458
 0.1201
P684 ortholog 3,430
 0.0131
P646 Freebase ID 3,160
 0.0007
P699 Disease Ontology ID 3,000
 0.1954
P5008 on focus list of Wikimedia project 2,717
 0.0041
P1550 Orphanet ID 2,614
 0.1797
P4229 ICD-10-CM 2,511
 0.1784
P6366 Microsoft Academic ID 2,181
 0.0079
P486 MeSH descriptor ID 2,127
 0.0499
P692 Gene Atlas Image 1,913
 0.1310
P4317 GARD rare disease ID 1,799
 0.1628
P1995 health specialty 1,460
 0.0989
P665 KEGG ID 1,452
 0.0552
P18 image 1,344
 0.0003
P1748 NCI Thesaurus ID 1,204
 0.0757
P7807 ICD-11 (foundation) 930
 0.0541
P557 DiseasesDB 864
 0.0871
P10283 OpenAlex ID 864
 0.0081
P2671 Google Knowledge Graph ID 831
 0.0001
P1692 ICD-9-CM 672
 0.0597
P672 MeSH tree code 661
 0.0280
P7464 Genetics Home Reference Conditions ID 573
 0.0719
P373 Commons category 571
 0.0002
P673 eMedicine ID 495
 0.0499
P7329 ID (MMS) 478
 0.0314
P1417 Encyclopædia Britannica Online ID 429
 0.0024
P494 ICD-10 417
 0.0350
P493 ICD-9 405
 0.0358
P3827 JSTOR topic ID 369
 0.0113
P604 MedlinePlus ID 344
 0.0365

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P492 OMIM ID 7,355
 0.2963
P699 Disease Ontology ID 3,000
 0.1954
P1550 Orphanet ID 2,614
 0.1797
P4229 ICD-10-CM 2,511
 0.1784
P5270 MonDO ID 3,572
 0.1642
P4317 GARD rare disease ID 1,799
 0.1628
P2892 UMLS CUI 3,790
 0.1320
P692 Gene Atlas Image 1,913
 0.1310
P5572 expressed in 3,458
 0.1201
P1995 health specialty 1,460
 0.0989
P557 DiseasesDB 864
 0.0871
P1748 NCI Thesaurus ID 1,204
 0.0757
P354 HGNC ID 3,527
 0.0738
P353 HGNC gene symbol 3,528
 0.0736
P7464 Genetics Home Reference Conditions ID 573
 0.0719
P1692 ICD-9-CM 672
 0.0597
P665 KEGG ID 1,452
 0.0552
P7807 ICD-11 (foundation) 930
 0.0541
P673 eMedicine ID 495
 0.0499
P486 MeSH descriptor ID 2,127
 0.0499
P604 MedlinePlus ID 344
 0.0365
P493 ICD-9 405
 0.0358
P494 ICD-10 417
 0.0350
P3841 Human Phenotype Ontology ID 321
 0.0347
P593 HomoloGene ID 3,491
 0.0334
P7329 ID (MMS) 478
 0.0314
P672 MeSH tree code 661
 0.0280
P780 symptoms and signs 250
 0.0270
P2176 drug or therapy used for treatment 234
 0.0265
P704 Ensembl transcript ID 3,469
 0.0248
P594 Ensembl gene ID 3,521
 0.0227
P1461 Patientplus ID 179
 0.0214
P5806 SNOMED CT identifier 165
 0.0196
P4196 cytogenetic location 3,482
 0.0183
P667 ICPC 2 ID 157
 0.0183
P7995 NHS Health A to Z ID 146
 0.0179
P3471 WikiSkripta ID 167
 0.0168
P668 GeneReviews ID 121
 0.0155
P5082 Store medisinske leksikon ID 163
 0.0154
P684 ortholog 3,430
 0.0131
P639 RefSeq RNA ID 3,518
 0.0130
P3827 JSTOR topic ID 369
 0.0113
P10283 OpenAlex ID 864
 0.0081
P6366 Microsoft Academic ID 2,181
 0.0079
P563 ICD-O 65
 0.0075
P508 BNCF Thesaurus ID 174
 0.0073
P1193 prevalence 56
 0.0072
P923 medical examinations 55
 0.0068
P924 possible treatment 54
 0.0067
P9272 DeCS ID 58
 0.0061