As of 2022-03-07, the Wikidata property comorbidity (P7500) is used on 9 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
P1995 health specialty 9
0.0011
P2892 UMLS CUI 9
0.0004
P279 subclass of 9
0.0000
P1550 Orphanet ID 8
0.0009
P2888 exact match 8
0.0000
P4317 GARD rare disease ID 7
0.0014
P7807 ICD-11 (foundation) 7
0.0007
P699 Disease Ontology ID 7
0.0007
P492 OMIM ID 7
0.0003
P486 MeSH descriptor ID 7
0.0002
P3417 Quora topic ID 7
0.0000
P5008 on focus list of Wikimedia project 7
0.0000
P2176 drug or therapy used for treatment 6
0.0046
P557 DiseasesDB 6
0.0020
P4229 ICD-10-CM 6
0.0007
P1748 NCI Thesaurus ID 6
0.0006
P10283 OpenAlex ID 6
0.0001
P646 Freebase ID 6
0.0000
P31 instance of 6
0.0000
P604 MedlinePlus ID 5
0.0025
P2293 genetic association 5
0.0006
P672 MeSH tree code 5
0.0003
P5270 MonDO ID 5
0.0003
P6366 Microsoft Academic ID 5
0.0000
P673 eMedicine ID 4
0.0015
P7329 ID (MMS) 4
0.0005
P665 KEGG ID 4
0.0002
P3827 JSTOR topic ID 4
0.0002
P8408 KBpedia ID 4
0.0001
P1417 Encyclopædia Britannica Online ID 4
0.0000
P373 Commons category 4
0.0000
P18 image 4
0.0000
P1461 Patientplus ID 3
0.0039
P667 ICPC 2 ID 3
0.0032
P493 ICD-9 3
0.0008
P1692 ICD-9-CM 3
0.0007
P494 ICD-10 3
0.0007
P508 BNCF Thesaurus ID 3
0.0002
P349 National Diet Library ID 3
0.0000
P8189 National Library of Israel J9U ID 3
0.0000
P138 named after 3
0.0000
P244 Library of Congress authority ID 3
0.0000
P924 possible treatment 2
0.0064
P10376 ScienceDirect topic ID 2
0.0012
P828 has cause 2
0.0003
P461 opposite of 2
0.0001
P2347 YSO ID 2
0.0001
P1368 LNB ID 2
0.0000
P443 pronunciation audio 2
0.0000
P61 discoverer or inventor 2
0.0000

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P5085 Pschyrembel Online ID 1
0.0303
P924 possible treatment 2
0.0064
P2176 drug or therapy used for treatment 6
0.0046
P1461 Patientplus ID 3
0.0039
P667 ICPC 2 ID 3
0.0032
P604 MedlinePlus ID 5
0.0025
P9123 Catalan Vikidia ID 1
0.0021
P557 DiseasesDB 6
0.0020
P920 LEM ID 1
0.0019
P7995 NHS Health A to Z ID 1
0.0018
P673 eMedicine ID 4
0.0015
P4317 GARD rare disease ID 7
0.0014
P7464 Genetics Home Reference Conditions ID 1
0.0013
P10376 ScienceDirect topic ID 2
0.0012
P8785 AniDB tag ID 1
0.0012
P1995 health specialty 9
0.0011
P1550 Orphanet ID 8
0.0009
P493 ICD-9 3
0.0008
P1692 ICD-9-CM 3
0.0007
P3509 Dagens Nyheter topic ID 1
0.0007
P4229 ICD-10-CM 6
0.0007
P7807 ICD-11 (foundation) 7
0.0007
P5737 Chinese Moegirlpedia ID 1
0.0007
P699 Disease Ontology ID 7
0.0007
P494 ICD-10 3
0.0007
P1748 NCI Thesaurus ID 6
0.0006
P2293 genetic association 5
0.0006
P9272 DeCS ID 1
0.0006
P3841 Human Phenotype Ontology ID 1
0.0006
P7329 ID (MMS) 4
0.0005
P2184 history of topic 1
0.0005
P3471 WikiSkripta ID 1
0.0004
P6293 YSA ID 1
0.0004
P3221 New York Times topic ID 1
0.0004
P2892 UMLS CUI 9
0.0004
P5082 Store medisinske leksikon ID 1
0.0003
P8885 Namuwiki ID 1
0.0003
P672 MeSH tree code 5
0.0003
P492 OMIM ID 7
0.0003
P5270 MonDO ID 5
0.0003
P828 has cause 2
0.0003
P1256 Iconclass notation 1
0.0003
P8309 Yle topic ID 1
0.0003
P2572 hashtag 1
0.0002
P9545 Encyclopedia of China Online Database ID 1
0.0002
P2579 studied by 1
0.0002
P665 KEGG ID 4
0.0002
P3569 Cultureel Woordenboek ID 1
0.0002
P486 MeSH descriptor ID 7
0.0002
P508 BNCF Thesaurus ID 3
0.0002