As of 2022-03-07, the Wikidata property has phenotype (P6532) is used on 99 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 99
 0.0000
P2888 exact match 98
 0.0000
P699 Disease Ontology ID 95
 0.0090
P5008 on focus list of Wikimedia project 94
 0.0001
P2892 UMLS CUI 84
 0.0034
P5270 MonDO ID 77
 0.0044
P1995 health specialty 67
 0.0079
P1550 Orphanet ID 66
 0.0070
P486 MeSH descriptor ID 64
 0.0017
P31 instance of 64
 0.0000
P4229 ICD-10-CM 63
 0.0071
P492 OMIM ID 61
 0.0025
P6366 Microsoft Academic ID 60
 0.0002
P1748 NCI Thesaurus ID 59
 0.0063
P4317 GARD rare disease ID 57
 0.0111
P7807 ICD-11 (foundation) 53
 0.0051
P557 DiseasesDB 49
 0.0160
P2293 genetic association 46
 0.0059
P1692 ICD-9-CM 45
 0.0107
P646 Freebase ID 45
 0.0000
P672 MeSH tree code 43
 0.0026
P7329 ID (MMS) 39
 0.0049
P780 symptoms and signs 37
 0.0205
P665 KEGG ID 34
 0.0017
P373 Commons category 32
 0.0000
P673 eMedicine ID 31
 0.0115
P10283 OpenAlex ID 30
 0.0003
P3827 JSTOR topic ID 27
 0.0011
P494 ICD-10 25
 0.0054
P1417 Encyclopædia Britannica Online ID 24
 0.0001
P604 MedlinePlus ID 21
 0.0102
P18 image 21
 0.0000
P493 ICD-9 19
 0.0047
P2176 drug or therapy used for treatment 18
 0.0131
P7464 Genetics Home Reference Conditions ID 17
 0.0201
P927 anatomical location 11
 0.0038
P828 has cause 11
 0.0014
P508 BNCF Thesaurus ID 11
 0.0007
P2581 BabelNet ID 11
 0.0002
P244 Library of Congress authority ID 11
 0.0000
P1461 Patientplus ID 10
 0.0118
P5082 Store medisinske leksikon ID 10
 0.0033
P8408 KBpedia ID 10
 0.0003
P3417 Quora topic ID 10
 0.0001
P138 named after 10
 0.0000
P3841 Human Phenotype Ontology ID 8
 0.0043
P1325 external data available at 8
 0.0004
P8189 National Library of Israel J9U ID 8
 0.0000
P268 Bibliothèque nationale de France ID 8
 0.0000
P1060 pathogen transmission process 7
 0.0238

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P1060 pathogen transmission process 7
 0.0238
P780 symptoms and signs 37
 0.0205
P7464 Genetics Home Reference Conditions ID 17
 0.0201
P5131 possible medical findings 3
 0.0189
P923 medical examinations 7
 0.0166
P1193 prevalence 3
 0.0163
P557 DiseasesDB 49
 0.0160
P924 possible treatment 6
 0.0150
P3487 maximal incubation period in humans 3
 0.0143
P3488 minimal incubation period in humans 3
 0.0142
P1605 has natural reservoir 3
 0.0137
P2176 drug or therapy used for treatment 18
 0.0131
P1461 Patientplus ID 10
 0.0118
P673 eMedicine ID 31
 0.0115
P4317 GARD rare disease ID 57
 0.0111
P7995 NHS Health A to Z ID 7
 0.0111
P1692 ICD-9-CM 45
 0.0107
P604 MedlinePlus ID 21
 0.0102
P7738 EEPS ID 1
 0.0099
P8016 Encyclopédie sur le développement des jeunes enfants ID 1
 0.0099
P653 PubMed Health 1
 0.0095
P9353 does not have cause 1
 0.0093
P6531 observed in 1
 0.0090
P699 Disease Ontology ID 95
 0.0090
P6223 L'Encyclopédie philosophique ID 1
 0.0085
P6530 has role in modeling 1
 0.0085
P1995 health specialty 67
 0.0079
P5806 SNOMED CT identifier 7
 0.0077
P8015 Encyclopedia on Early Childhood Development ID (English) 1
 0.0071
P4229 ICD-10-CM 63
 0.0071
P1550 Orphanet ID 66
 0.0070
P7889 Cambridge Encyclopedia of Anthropology ID 1
 0.0063
P1748 NCI Thesaurus ID 59
 0.0063
P2293 genetic association 46
 0.0059
P667 ICPC 2 ID 6
 0.0058
P10022 Dizionario di Medicina ID 1
 0.0056
P494 ICD-10 25
 0.0054
P7807 ICD-11 (foundation) 53
 0.0051
P7329 ID (MMS) 39
 0.0049
P493 ICD-9 19
 0.0047
P5642 risk factor 1
 0.0046
P5270 MonDO ID 77
 0.0044
P3841 Human Phenotype Ontology ID 8
 0.0043
P668 GeneReviews ID 1
 0.0040
P927 anatomical location 11
 0.0038
P3720 GPnotebook ID 2
 0.0037
P2892 UMLS CUI 84
 0.0034
P5082 Store medisinske leksikon ID 10
 0.0033
P9827 GSSO ID 1
 0.0027
P672 MeSH tree code 43
 0.0026