As of 2022-03-07, the Wikidata property MonDO ID (P5270) is used on 17,545 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 16,467
 0.0062
P2888 exact match 14,504
 0.0045
P2892 UMLS CUI 13,564
 0.4724
P1550 Orphanet ID 8,325
 0.4475
P5008 on focus list of Wikimedia project 8,124
 0.0121
P699 Disease Ontology ID 8,112
 0.4055
P4229 ICD-10-CM 8,069
 0.4412
P31 instance of 8,041
 0.0001
P492 OMIM ID 6,783
 0.1929
P486 MeSH descriptor ID 6,470
 0.1347
P1748 NCI Thesaurus ID 5,747
 0.2720
P1995 health specialty 4,882
 0.2312
P4317 GARD rare disease ID 4,047
 0.2179
P7807 ICD-11 (foundation) 3,995
 0.1673
P1692 ICD-9-CM 3,639
 0.2015
P2293 genetic association 3,572
 0.1642
P6366 Microsoft Academic ID 3,149
 0.0111
P7329 ID (MMS) 2,699
 0.1186
P672 MeSH tree code 2,595
 0.0826
P646 Freebase ID 1,937
 0.0004
P557 DiseasesDB 1,816
 0.0969
P665 KEGG ID 1,760
 0.0492
P10283 OpenAlex ID 1,736
 0.0150
P373 Commons category 1,672
 0.0005
P494 ICD-10 1,510
 0.0733
P673 eMedicine ID 1,299
 0.0688
P3827 JSTOR topic ID 1,267
 0.0305
P493 ICD-9 1,226
 0.0605
P1417 Encyclopædia Britannica Online ID 1,111
 0.0059
P3841 Human Phenotype Ontology ID 1,076
 0.0590
P927 anatomical location 1,069
 0.0555
P18 image 981
 0.0002
P2176 drug or therapy used for treatment 945
 0.0528
P604 MedlinePlus ID 934
 0.0502
P780 symptoms and signs 713
 0.0384
P3417 Quora topic ID 686
 0.0034
P828 has cause 649
 0.0265
P563 ICD-O 622
 0.0348
P7464 Genetics Home Reference Conditions ID 558
 0.0314
P2671 Google Knowledge Graph ID 548
 0.0001
P244 Library of Congress authority ID 537
 0.0004
P508 BNCF Thesaurus ID 521
 0.0156
P5082 Store medisinske leksikon ID 510
 0.0255
P910 topic's main category 501
 0.0007
P2581 BabelNet ID 488
 0.0054
P667 ICPC 2 ID 462
 0.0256
P8408 KBpedia ID 428
 0.0077
P5806 SNOMED CT identifier 427
 0.0238
P1296 Gran Enciclopèdia Catalana ID 406
 0.0031
P1461 Patientplus ID 393
 0.0219

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P2892 UMLS CUI 13,564
 0.4724
P1550 Orphanet ID 8,325
 0.4475
P4229 ICD-10-CM 8,069
 0.4412
P699 Disease Ontology ID 8,112
 0.4055
P1748 NCI Thesaurus ID 5,747
 0.2720
P1995 health specialty 4,882
 0.2312
P4317 GARD rare disease ID 4,047
 0.2179
P1692 ICD-9-CM 3,639
 0.2015
P492 OMIM ID 6,783
 0.1929
P7807 ICD-11 (foundation) 3,995
 0.1673
P2293 genetic association 3,572
 0.1642
P486 MeSH descriptor ID 6,470
 0.1347
P7329 ID (MMS) 2,699
 0.1186
P557 DiseasesDB 1,816
 0.0969
P672 MeSH tree code 2,595
 0.0826
P494 ICD-10 1,510
 0.0733
P673 eMedicine ID 1,299
 0.0688
P493 ICD-9 1,226
 0.0605
P3841 Human Phenotype Ontology ID 1,076
 0.0590
P927 anatomical location 1,069
 0.0555
P2176 drug or therapy used for treatment 945
 0.0528
P604 MedlinePlus ID 934
 0.0502
P665 KEGG ID 1,760
 0.0492
P780 symptoms and signs 713
 0.0384
P563 ICD-O 622
 0.0348
P7464 Genetics Home Reference Conditions ID 558
 0.0314
P3827 JSTOR topic ID 1,267
 0.0305
P828 has cause 649
 0.0265
P667 ICPC 2 ID 462
 0.0256
P5082 Store medisinske leksikon ID 510
 0.0255
P5806 SNOMED CT identifier 427
 0.0238
P1461 Patientplus ID 393
 0.0219
P3471 WikiSkripta ID 386
 0.0198
P7995 NHS Health A to Z ID 314
 0.0177
P508 BNCF Thesaurus ID 521
 0.0156
P10283 OpenAlex ID 1,736
 0.0150
P5008 on focus list of Wikimedia project 8,124
 0.0121
P4746 Elhuyar ZTH ID 274
 0.0115
P923 medical examinations 197
 0.0111
P6366 Microsoft Academic ID 3,149
 0.0111
P689 afflicts 202
 0.0108
P2004 NALT ID 226
 0.0095
P924 possible treatment 159
 0.0090
P2347 YSO ID 361
 0.0088
P1060 pathogen transmission process 143
 0.0081
P8408 KBpedia ID 428
 0.0077
P1245 OmegaWiki Defined Meaning 213
 0.0074
P279 subclass of 16,467
 0.0062
P1325 external data available at 222
 0.0060
P1417 Encyclopædia Britannica Online ID 1,111
 0.0059