As of 2022-03-07, the Wikidata property GARD rare disease ID (P4317) is used on 5,074 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 4,827
 0.0018
P2892 UMLS CUI 4,134
 0.1610
P5270 MonDO ID 4,047
 0.2179
P2888 exact match 4,020
 0.0012
P1550 Orphanet ID 3,454
 0.3139
P486 MeSH descriptor ID 3,208
 0.0826
P31 instance of 3,118
 0.0000
P492 OMIM ID 3,043
 0.1151
P4229 ICD-10-CM 2,957
 0.2706
P699 Disease Ontology ID 2,590
 0.1983
P5008 on focus list of Wikimedia project 2,466
 0.0037
P1995 health specialty 2,077
 0.1814
P6366 Microsoft Academic ID 2,058
 0.0075
P1748 NCI Thesaurus ID 1,810
 0.1437
P2293 genetic association 1,799
 0.1628
P7807 ICD-11 (foundation) 1,788
 0.1313
P557 DiseasesDB 1,422
 0.2135
P665 KEGG ID 1,419
 0.0601
P646 Freebase ID 1,268
 0.0003
P672 MeSH tree code 1,222
 0.0602
P1692 ICD-9-CM 1,210
 0.1508
P7329 ID (MMS) 1,088
 0.0914
P10283 OpenAlex ID 994
 0.0095
P373 Commons category 982
 0.0003
P673 eMedicine ID 938
 0.1387
P494 ICD-10 858
 0.0978
P493 ICD-9 796
 0.0969
P7464 Genetics Home Reference Conditions ID 650
 0.1253
P3827 JSTOR topic ID 643
 0.0217
P18 image 596
 0.0001
P1417 Encyclopædia Britannica Online ID 578
 0.0033
P604 MedlinePlus ID 576
 0.0889
P3841 Human Phenotype Ontology ID 473
 0.0741
P780 symptoms and signs 400
 0.0624
P2176 drug or therapy used for treatment 397
 0.0664
P3417 Quora topic ID 390
 0.0021
P138 named after 296
 0.0009
P1461 Patientplus ID 279
 0.0503
P2671 Google Knowledge Graph ID 273
 0.0000
P2581 BabelNet ID 271
 0.0035
P5806 SNOMED CT identifier 264
 0.0470
P1325 external data available at 254
 0.0105
P3471 WikiSkripta ID 249
 0.0348
P244 Library of Congress authority ID 244
 0.0002
P828 has cause 243
 0.0196
P508 BNCF Thesaurus ID 242
 0.0114
P563 ICD-O 236
 0.0408
P5082 Store medisinske leksikon ID 228
 0.0292
P667 ICPC 2 ID 207
 0.0356
P1296 Gran Enciclopèdia Catalana ID 196
 0.0016

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P1550 Orphanet ID 3,454
 0.3139
P4229 ICD-10-CM 2,957
 0.2706
P5270 MonDO ID 4,047
 0.2179
P557 DiseasesDB 1,422
 0.2135
P699 Disease Ontology ID 2,590
 0.1983
P1995 health specialty 2,077
 0.1814
P2293 genetic association 1,799
 0.1628
P2892 UMLS CUI 4,134
 0.1610
P1692 ICD-9-CM 1,210
 0.1508
P1748 NCI Thesaurus ID 1,810
 0.1437
P673 eMedicine ID 938
 0.1387
P7807 ICD-11 (foundation) 1,788
 0.1313
P7464 Genetics Home Reference Conditions ID 650
 0.1253
P492 OMIM ID 3,043
 0.1151
P494 ICD-10 858
 0.0978
P493 ICD-9 796
 0.0969
P7329 ID (MMS) 1,088
 0.0914
P604 MedlinePlus ID 576
 0.0889
P486 MeSH descriptor ID 3,208
 0.0826
P3841 Human Phenotype Ontology ID 473
 0.0741
P2176 drug or therapy used for treatment 397
 0.0664
P780 symptoms and signs 400
 0.0624
P672 MeSH tree code 1,222
 0.0602
P665 KEGG ID 1,419
 0.0601
P1461 Patientplus ID 279
 0.0503
P5806 SNOMED CT identifier 264
 0.0470
P563 ICD-O 236
 0.0408
P667 ICPC 2 ID 207
 0.0356
P7995 NHS Health A to Z ID 193
 0.0356
P3471 WikiSkripta ID 249
 0.0348
P5082 Store medisinske leksikon ID 228
 0.0292
P668 GeneReviews ID 140
 0.0275
P923 medical examinations 123
 0.0233
P3827 JSTOR topic ID 643
 0.0217
P828 has cause 243
 0.0196
P927 anatomical location 148
 0.0192
P924 possible treatment 81
 0.0153
P9272 DeCS ID 98
 0.0146
P1060 pathogen transmission process 73
 0.0140
P1193 prevalence 63
 0.0124
P3487 maximal incubation period in humans 59
 0.0115
P3488 minimal incubation period in humans 59
 0.0115
P508 BNCF Thesaurus ID 242
 0.0114
P6532 has phenotype 57
 0.0111
P1325 external data available at 254
 0.0105
P1199 mode of inheritance 50
 0.0098
P10283 OpenAlex ID 994
 0.0095
P4746 Elhuyar ZTH ID 96
 0.0083
P2004 NALT ID 89
 0.0077
P689 afflicts 48
 0.0076