As of 2022-03-07, the Wikidata property GeneReviews ID (P668) is used on 151 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 150
 0.0001
P492 OMIM ID 142
 0.0058
P2888 exact match 142
 0.0000
P4317 GARD rare disease ID 140
 0.0275
P2892 UMLS CUI 138
 0.0056
P557 DiseasesDB 137
 0.0453
P1550 Orphanet ID 137
 0.0146
P1995 health specialty 134
 0.0158
P699 Disease Ontology ID 134
 0.0127
P5008 on focus list of Wikimedia project 132
 0.0002
P31 instance of 132
 0.0000
P665 KEGG ID 130
 0.0065
P6366 Microsoft Academic ID 129
 0.0005
P1748 NCI Thesaurus ID 122
 0.0130
P2293 genetic association 121
 0.0155
P486 MeSH descriptor ID 120
 0.0032
P4229 ICD-10-CM 116
 0.0131
P646 Freebase ID 107
 0.0000
P5270 MonDO ID 99
 0.0056
P7807 ICD-11 (foundation) 94
 0.0091
P7464 Genetics Home Reference Conditions ID 92
 0.1121
P672 MeSH tree code 92
 0.0056
P673 eMedicine ID 81
 0.0300
P10283 OpenAlex ID 79
 0.0008
P7329 ID (MMS) 67
 0.0084
P493 ICD-9 66
 0.0164
P373 Commons category 65
 0.0000
P1692 ICD-9-CM 62
 0.0146
P1417 Encyclopædia Britannica Online ID 58
 0.0003
P604 MedlinePlus ID 56
 0.0270
P3827 JSTOR topic ID 46
 0.0018
P494 ICD-10 40
 0.0086
P3417 Quora topic ID 40
 0.0002
P18 image 40
 0.0000
P138 named after 36
 0.0001
P1325 external data available at 33
 0.0017
P1461 Patientplus ID 29
 0.0331
P780 symptoms and signs 28
 0.0150
P3841 Human Phenotype Ontology ID 28
 0.0147
P2176 drug or therapy used for treatment 26
 0.0183
P1193 prevalence 21
 0.0963
P7995 NHS Health A to Z ID 20
 0.0298
P5806 SNOMED CT identifier 19
 0.0201
P667 ICPC 2 ID 19
 0.0177
P3471 WikiSkripta ID 18
 0.0073
P508 BNCF Thesaurus ID 18
 0.0011
P2347 YSO ID 18
 0.0008
P244 Library of Congress authority ID 18
 0.0000
P828 has cause 17
 0.0022
P3219 Encyclopædia Universalis ID 17
 0.0005

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P7464 Genetics Home Reference Conditions ID 92
 0.1121
P1193 prevalence 21
 0.0963
P557 DiseasesDB 137
 0.0453
P1199 mode of inheritance 10
 0.0444
P923 medical examinations 16
 0.0345
P1461 Patientplus ID 29
 0.0331
P924 possible treatment 14
 0.0315
P673 eMedicine ID 81
 0.0300
P7995 NHS Health A to Z ID 20
 0.0298
P4317 GARD rare disease ID 140
 0.0275
P604 MedlinePlus ID 56
 0.0270
P5806 SNOMED CT identifier 19
 0.0201
P2176 drug or therapy used for treatment 26
 0.0183
P667 ICPC 2 ID 19
 0.0177
P493 ICD-9 66
 0.0164
P1995 health specialty 134
 0.0158
P2293 genetic association 121
 0.0155
P780 symptoms and signs 28
 0.0150
P3841 Human Phenotype Ontology ID 28
 0.0147
P1692 ICD-9-CM 62
 0.0146
P1550 Orphanet ID 137
 0.0146
P4229 ICD-10-CM 116
 0.0131
P1748 NCI Thesaurus ID 122
 0.0130
P699 Disease Ontology ID 134
 0.0127
P5131 possible medical findings 2
 0.0094
P7807 ICD-11 (foundation) 94
 0.0091
P494 ICD-10 40
 0.0086
P7329 ID (MMS) 67
 0.0084
P3471 WikiSkripta ID 18
 0.0073
P7738 EEPS ID 1
 0.0065
P8016 Encyclopédie sur le développement des jeunes enfants ID 1
 0.0065
P665 KEGG ID 130
 0.0065
P9272 DeCS ID 12
 0.0065
P653 PubMed Health 1
 0.0064
P8401 TheFreeDictionary medical term ID 1
 0.0063
P9353 does not have cause 1
 0.0063
P6223 L'Encyclopédie philosophique ID 1
 0.0059
P492 OMIM ID 142
 0.0058
P5270 MonDO ID 99
 0.0056
P2892 UMLS CUI 138
 0.0056
P672 MeSH tree code 92
 0.0056
P8015 Encyclopedia on Early Childhood Development ID (English) 1
 0.0052
P1583 MalaCards ID 1
 0.0051
P7889 Cambridge Encyclopedia of Anthropology ID 1
 0.0048
P10022 Dizionario di Medicina ID 1
 0.0044
P6532 has phenotype 1
 0.0040
P486 MeSH descriptor ID 120
 0.0032
P9346 France24 topic ID (French) 1
 0.0031
P5082 Store medisinske leksikon ID 9
 0.0029
P6417 Homosaurus ID (V2) 2
 0.0028