As of 2022-03-07, the Wikidata property mode of inheritance (P1199) is used on 84 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 81
 0.0000
P2888 exact match 70
 0.0000
P1550 Orphanet ID 67
 0.0071
P492 OMIM ID 63
 0.0026
P5270 MonDO ID 61
 0.0035
P2892 UMLS CUI 60
 0.0024
P4229 ICD-10-CM 58
 0.0066
P486 MeSH descriptor ID 58
 0.0016
P31 instance of 57
 0.0000
P4317 GARD rare disease ID 50
 0.0098
P699 Disease Ontology ID 50
 0.0047
P5008 on focus list of Wikimedia project 47
 0.0001
P1995 health specialty 41
 0.0048
P2293 genetic association 37
 0.0047
P557 DiseasesDB 34
 0.0111
P665 KEGG ID 33
 0.0016
P1748 NCI Thesaurus ID 31
 0.0033
P7807 ICD-11 (foundation) 31
 0.0030
P646 Freebase ID 30
 0.0000
P672 MeSH tree code 28
 0.0017
P6366 Microsoft Academic ID 28
 0.0001
P673 eMedicine ID 27
 0.0101
P493 ICD-9 21
 0.0052
P373 Commons category 21
 0.0000
P3827 JSTOR topic ID 19
 0.0008
P7464 Genetics Home Reference Conditions ID 18
 0.0217
P1692 ICD-9-CM 18
 0.0043
P10283 OpenAlex ID 18
 0.0002
P1417 Encyclopædia Britannica Online ID 18
 0.0001
P604 MedlinePlus ID 17
 0.0083
P7329 ID (MMS) 15
 0.0019
P494 ICD-10 12
 0.0026
P18 image 12
 0.0000
P668 GeneReviews ID 10
 0.0444
P1461 Patientplus ID 9
 0.0108
P2176 drug or therapy used for treatment 8
 0.0058
P3219 Encyclopædia Universalis ID 8
 0.0002
P2581 BabelNet ID 8
 0.0001
P3417 Quora topic ID 8
 0.0000
P780 symptoms and signs 7
 0.0039
P828 has cause 7
 0.0009
P667 ICPC 2 ID 6
 0.0059
P508 BNCF Thesaurus ID 6
 0.0004
P138 named after 6
 0.0000
P1325 external data available at 5
 0.0003
P4527 UK Parliament thesaurus ID 5
 0.0002
P910 topic's main category 5
 0.0000
P2671 Google Knowledge Graph ID 5
 0.0000
P1193 prevalence 4
 0.0238
P7995 NHS Health A to Z ID 4
 0.0064

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P668 GeneReviews ID 10
 0.0444
P1193 prevalence 4
 0.0238
P7464 Genetics Home Reference Conditions ID 18
 0.0217
P1929 ClinVar Variation ID 1
 0.0116
P557 DiseasesDB 34
 0.0111
P653 PubMed Health 1
 0.0111
P1461 Patientplus ID 9
 0.0108
P673 eMedicine ID 27
 0.0101
P6861 dbSNP ID 1
 0.0099
P4317 GARD rare disease ID 50
 0.0098
P604 MedlinePlus ID 17
 0.0083
P1583 MalaCards ID 1
 0.0078
P923 medical examinations 3
 0.0073
P1550 Orphanet ID 67
 0.0071
P5131 possible medical findings 1
 0.0068
P4229 ICD-10-CM 58
 0.0066
P7995 NHS Health A to Z ID 4
 0.0064
P667 ICPC 2 ID 6
 0.0059
P2176 drug or therapy used for treatment 8
 0.0058
P493 ICD-9 21
 0.0052
P924 possible treatment 2
 0.0051
P5642 risk factor 1
 0.0050
P1995 health specialty 41
 0.0048
P2293 genetic association 37
 0.0047
P699 Disease Ontology ID 50
 0.0047
P1692 ICD-9-CM 18
 0.0043
P780 symptoms and signs 7
 0.0039
P5270 MonDO ID 61
 0.0035
P8285 LGBT Danmark online dictionary ID 1
 0.0035
P1748 NCI Thesaurus ID 31
 0.0033
P7807 ICD-11 (foundation) 31
 0.0030
P494 ICD-10 12
 0.0026
P492 OMIM ID 63
 0.0026
P2892 UMLS CUI 60
 0.0024
P5806 SNOMED CT identifier 2
 0.0022
P805 statement is subject of 1
 0.0022
P3720 GPnotebook ID 1
 0.0019
P7329 ID (MMS) 15
 0.0019
P672 MeSH tree code 28
 0.0017
P3471 WikiSkripta ID 4
 0.0017
P665 KEGG ID 33
 0.0016
P3841 Human Phenotype Ontology ID 3
 0.0016
P486 MeSH descriptor ID 58
 0.0016
P6417 Homosaurus ID (V2) 1
 0.0016
P3331 HGVS nomenclature 1
 0.0010
P5082 Store medisinske leksikon ID 3
 0.0010
P828 has cause 7
 0.0009
P3827 JSTOR topic ID 19
 0.0008
P3885 History of Modern Biomedicine ID 1
 0.0007
P9272 DeCS ID 1
 0.0006