As of 2022-03-07, the Wikidata property OMIM ID (P492) is used on 24,402 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 23,707
 0.0089
P2888 exact match 22,443
 0.0069
P31 instance of 20,928
 0.0002
P703 found in taxon 16,023
 0.0062
P351 Entrez Gene ID 16,016
 0.0203
P353 HGNC gene symbol 15,983
 0.3066
P354 HGNC ID 15,978
 0.3076
P639 RefSeq RNA ID 15,825
 0.0574
P4196 cytogenetic location 15,822
 0.0815
P594 Ensembl gene ID 15,795
 0.0990
P1057 chromosome 15,517
 0.0251
P704 Ensembl transcript ID 15,486
 0.1071
P644 genomic start 15,484
 0.0150
P645 genomic end 15,484
 0.0150
P2548 strand orientation 15,476
 0.0150
P5572 expressed in 15,357
 0.4583
P688 encodes 15,199
 0.0157
P593 HomoloGene ID 15,013
 0.1370
P684 ortholog 14,190
 0.0530
P646 Freebase ID 10,939
 0.0025
P692 Gene Atlas Image 7,384
 0.2866
P2293 genetic association 7,355
 0.2963
P2892 UMLS CUI 7,272
 0.1737
P5270 MonDO ID 6,783
 0.1929
P6366 Microsoft Academic ID 4,918
 0.0170
P486 MeSH descriptor ID 4,499
 0.0791
P2671 Google Knowledge Graph ID 4,344
 0.0006
P699 Disease Ontology ID 4,251
 0.1384
P1550 Orphanet ID 4,237
 0.1434
P18 image 3,894
 0.0009
P5008 on focus list of Wikimedia project 3,836
 0.0056
P4229 ICD-10-CM 3,723
 0.1262
P4317 GARD rare disease ID 3,043
 0.1151
P1995 health specialty 2,038
 0.0661
P665 KEGG ID 1,642
 0.0384
P1748 NCI Thesaurus ID 1,636
 0.0510
P10283 OpenAlex ID 1,574
 0.0128
P7807 ICD-11 (foundation) 1,468
 0.0441
P557 DiseasesDB 1,210
 0.0462
P1692 ICD-9-CM 978
 0.0355
P672 MeSH tree code 913
 0.0229
P373 Commons category 884
 0.0003
P7329 ID (MMS) 742
 0.0235
P673 eMedicine ID 727
 0.0276
P494 ICD-10 692
 0.0245
P7464 Genetics Home Reference Conditions ID 660
 0.0269
P493 ICD-9 658
 0.0238
P1417 Encyclopædia Britannica Online ID 581
 0.0030
P3841 Human Phenotype Ontology ID 540
 0.0211
P3827 JSTOR topic ID 506
 0.0103

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P5572 expressed in 15,357
 0.4583
P354 HGNC ID 15,978
 0.3076
P353 HGNC gene symbol 15,983
 0.3066
P2293 genetic association 7,355
 0.2963
P692 Gene Atlas Image 7,384
 0.2866
P5270 MonDO ID 6,783
 0.1929
P2892 UMLS CUI 7,272
 0.1737
P1550 Orphanet ID 4,237
 0.1434
P699 Disease Ontology ID 4,251
 0.1384
P593 HomoloGene ID 15,013
 0.1370
P4229 ICD-10-CM 3,723
 0.1262
P4317 GARD rare disease ID 3,043
 0.1151
P704 Ensembl transcript ID 15,486
 0.1071
P594 Ensembl gene ID 15,795
 0.0990
P4196 cytogenetic location 15,822
 0.0815
P486 MeSH descriptor ID 4,499
 0.0791
P1995 health specialty 2,038
 0.0661
P639 RefSeq RNA ID 15,825
 0.0574
P684 ortholog 14,190
 0.0530
P1748 NCI Thesaurus ID 1,636
 0.0510
P557 DiseasesDB 1,210
 0.0462
P7807 ICD-11 (foundation) 1,468
 0.0441
P665 KEGG ID 1,642
 0.0384
P1692 ICD-9-CM 978
 0.0355
P673 eMedicine ID 727
 0.0276
P7464 Genetics Home Reference Conditions ID 660
 0.0269
P1057 chromosome 15,517
 0.0251
P494 ICD-10 692
 0.0245
P493 ICD-9 658
 0.0238
P7329 ID (MMS) 742
 0.0235
P672 MeSH tree code 913
 0.0229
P3841 Human Phenotype Ontology ID 540
 0.0211
P351 Entrez Gene ID 16,016
 0.0203
P604 MedlinePlus ID 487
 0.0188
P6366 Microsoft Academic ID 4,918
 0.0170
P688 encodes 15,199
 0.0157
P2548 strand orientation 15,476
 0.0150
P644 genomic start 15,484
 0.0150
P645 genomic end 15,484
 0.0150
P10283 OpenAlex ID 1,574
 0.0128
P780 symptoms and signs 316
 0.0122
P2176 drug or therapy used for treatment 291
 0.0115
P3827 JSTOR topic ID 506
 0.0103
P1461 Patientplus ID 231
 0.0093
P5806 SNOMED CT identifier 227
 0.0091
P279 subclass of 23,707
 0.0089
P3471 WikiSkripta ID 217
 0.0082
P667 ICPC 2 ID 192
 0.0076
P5082 Store medisinske leksikon ID 203
 0.0075
P7995 NHS Health A to Z ID 180
 0.0073