As of 2022-03-07, the Wikidata property Orphanet ID (P1550) is used on 9,382 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
P2888 exact match 8,950
 0.0028
P279 subclass of 8,896
 0.0034
P5270 MonDO ID 8,325
 0.4475
P4229 ICD-10-CM 6,301
 0.5299
P2892 UMLS CUI 5,820
 0.2057
P31 instance of 5,472
 0.0001
P492 OMIM ID 4,237
 0.1434
P486 MeSH descriptor ID 3,596
 0.0841
P4317 GARD rare disease ID 3,454
 0.3139
P699 Disease Ontology ID 3,191
 0.1903
P5008 on focus list of Wikimedia project 2,978
 0.0045
P7807 ICD-11 (foundation) 2,617
 0.1531
P2293 genetic association 2,614
 0.1797
P1995 health specialty 2,305
 0.1484
P6366 Microsoft Academic ID 2,193
 0.0079
P1748 NCI Thesaurus ID 2,103
 0.1266
P665 KEGG ID 1,765
 0.0640
P7329 ID (MMS) 1,567
 0.0996
P1692 ICD-9-CM 1,394
 0.1148
P557 DiseasesDB 1,370
 0.1243
P672 MeSH tree code 1,238
 0.0503
P646 Freebase ID 1,224
 0.0003
P10283 OpenAlex ID 994
 0.0092
P494 ICD-10 968
 0.0746
P373 Commons category 957
 0.0003
P673 eMedicine ID 862
 0.0773
P493 ICD-9 810
 0.0647
P7464 Genetics Home Reference Conditions ID 669
 0.0706
P3827 JSTOR topic ID 610
 0.0180
P1417 Encyclopædia Britannica Online ID 586
 0.0033
P18 image 572
 0.0001
P3841 Human Phenotype Ontology ID 537
 0.0505
P604 MedlinePlus ID 518
 0.0478
P2671 Google Knowledge Graph ID 419
 0.0001
P2176 drug or therapy used for treatment 411
 0.0400
P780 symptoms and signs 403
 0.0376
P3417 Quora topic ID 357
 0.0019
P5806 SNOMED CT identifier 292
 0.0295
P563 ICD-O 277
 0.0276
P2581 BabelNet ID 277
 0.0034
P138 named after 276
 0.0008
P1325 external data available at 265
 0.0093
P1461 Patientplus ID 241
 0.0244
P244 Library of Congress authority ID 241
 0.0002
P828 has cause 233
 0.0140
P508 BNCF Thesaurus ID 229
 0.0090
P910 topic's main category 227
 0.0003
P3471 WikiSkripta ID 226
 0.0197
P5082 Store medisinske leksikon ID 214
 0.0177
P8408 KBpedia ID 214
 0.0045

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P4229 ICD-10-CM 6,301
 0.5299
P5270 MonDO ID 8,325
 0.4475
P4317 GARD rare disease ID 3,454
 0.3139
P2892 UMLS CUI 5,820
 0.2057
P699 Disease Ontology ID 3,191
 0.1903
P2293 genetic association 2,614
 0.1797
P7807 ICD-11 (foundation) 2,617
 0.1531
P1995 health specialty 2,305
 0.1484
P492 OMIM ID 4,237
 0.1434
P1748 NCI Thesaurus ID 2,103
 0.1266
P557 DiseasesDB 1,370
 0.1243
P1692 ICD-9-CM 1,394
 0.1148
P7329 ID (MMS) 1,567
 0.0996
P486 MeSH descriptor ID 3,596
 0.0841
P673 eMedicine ID 862
 0.0773
P494 ICD-10 968
 0.0746
P7464 Genetics Home Reference Conditions ID 669
 0.0706
P493 ICD-9 810
 0.0647
P665 KEGG ID 1,765
 0.0640
P3841 Human Phenotype Ontology ID 537
 0.0505
P672 MeSH tree code 1,238
 0.0503
P604 MedlinePlus ID 518
 0.0478
P2176 drug or therapy used for treatment 411
 0.0400
P780 symptoms and signs 403
 0.0376
P5806 SNOMED CT identifier 292
 0.0295
P563 ICD-O 277
 0.0276
P1461 Patientplus ID 241
 0.0244
P667 ICPC 2 ID 206
 0.0204
P3471 WikiSkripta ID 226
 0.0197
P3827 JSTOR topic ID 610
 0.0180
P5082 Store medisinske leksikon ID 214
 0.0177
P7995 NHS Health A to Z ID 167
 0.0171
P668 GeneReviews ID 137
 0.0146
P927 anatomical location 174
 0.0145
P828 has cause 233
 0.0140
P923 medical examinations 118
 0.0123
P1325 external data available at 265
 0.0093
P10283 OpenAlex ID 994
 0.0092
P508 BNCF Thesaurus ID 229
 0.0090
P1060 pathogen transmission process 82
 0.0086
P9272 DeCS ID 89
 0.0081
P6366 Microsoft Academic ID 2,193
 0.0079
P924 possible treatment 74
 0.0077
P1199 mode of inheritance 67
 0.0071
P6532 has phenotype 66
 0.0070
P3487 maximal incubation period in humans 60
 0.0064
P3488 minimal incubation period in humans 60
 0.0064
P2004 NALT ID 100
 0.0063
P1193 prevalence 59
 0.0063
P2347 YSO ID 185
 0.0056