As of 2022-03-07, the Wikidata property possible medical findings (P5131) is used on 63 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 54
 0.0000
P1995 health specialty 51
 0.0060
P2892 UMLS CUI 51
 0.0021
P7807 ICD-11 (foundation) 44
 0.0043
P2888 exact match 43
 0.0000
P31 instance of 43
 0.0000
P7329 ID (MMS) 41
 0.0052
P5008 on focus list of Wikimedia project 41
 0.0001
P373 Commons category 39
 0.0000
P557 DiseasesDB 38
 0.0125
P699 Disease Ontology ID 38
 0.0036
P646 Freebase ID 38
 0.0000
P673 eMedicine ID 37
 0.0139
P1748 NCI Thesaurus ID 37
 0.0040
P486 MeSH descriptor ID 37
 0.0010
P672 MeSH tree code 36
 0.0022
P10283 OpenAlex ID 36
 0.0004
P6366 Microsoft Academic ID 33
 0.0001
P604 MedlinePlus ID 32
 0.0159
P5270 MonDO ID 30
 0.0017
P3827 JSTOR topic ID 28
 0.0011
P3841 Human Phenotype Ontology ID 27
 0.0149
P1692 ICD-9-CM 26
 0.0062
P494 ICD-10 23
 0.0050
P4229 ICD-10-CM 23
 0.0026
P493 ICD-9 21
 0.0053
P18 image 21
 0.0000
P508 BNCF Thesaurus ID 19
 0.0012
P1417 Encyclopædia Britannica Online ID 19
 0.0001
P3471 WikiSkripta ID 16
 0.0067
P1550 Orphanet ID 16
 0.0017
P5082 Store medisinske leksikon ID 15
 0.0050
P4317 GARD rare disease ID 14
 0.0027
P665 KEGG ID 14
 0.0007
P2176 drug or therapy used for treatment 13
 0.0096
P927 anatomical location 13
 0.0046
P492 OMIM ID 13
 0.0005
P3417 Quora topic ID 13
 0.0001
P1461 Patientplus ID 12
 0.0149
P244 Library of Congress authority ID 12
 0.0000
P7995 NHS Health A to Z ID 11
 0.0185
P780 symptoms and signs 11
 0.0061
P268 Bibliothèque nationale de France ID 11
 0.0000
P667 ICPC 2 ID 10
 0.0101
P2293 genetic association 10
 0.0013
P1296 Gran Enciclopèdia Catalana ID 10
 0.0001
P1245 OmegaWiki Defined Meaning 9
 0.0008
P8189 National Library of Israel J9U ID 9
 0.0001
P5806 SNOMED CT identifier 8
 0.0092
P8408 KBpedia ID 8
 0.0002

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P6532 has phenotype 3
 0.0189
P7995 NHS Health A to Z ID 11
 0.0185
P923 medical examinations 7
 0.0182
P5642 risk factor 3
 0.0169
P924 possible treatment 6
 0.0165
P2074 internetmedicin.se ID 2
 0.0164
P604 MedlinePlus ID 32
 0.0159
P1461 Patientplus ID 12
 0.0149
P3841 Human Phenotype Ontology ID 27
 0.0149
P673 eMedicine ID 37
 0.0139
P1193 prevalence 2
 0.0134
P557 DiseasesDB 38
 0.0125
P667 ICPC 2 ID 10
 0.0101
P2176 drug or therapy used for treatment 13
 0.0096
P668 GeneReviews ID 2
 0.0094
P1583 MalaCards ID 1
 0.0093
P5806 SNOMED CT identifier 8
 0.0092
P10022 Dizionario di Medicina ID 1
 0.0071
P1199 mode of inheritance 1
 0.0068
P3471 WikiSkripta ID 16
 0.0067
P1692 ICD-9-CM 26
 0.0062
P780 symptoms and signs 11
 0.0061
P1995 health specialty 51
 0.0060
P3487 maximal incubation period in humans 1
 0.0057
P3488 minimal incubation period in humans 1
 0.0056
P1605 has natural reservoir 1
 0.0054
P493 ICD-9 21
 0.0053
P7329 ID (MMS) 41
 0.0052
P494 ICD-10 23
 0.0050
P5082 Store medisinske leksikon ID 15
 0.0050
P7464 Genetics Home Reference Conditions ID 4
 0.0049
P927 anatomical location 13
 0.0046
P8656 Symptom Ontology ID 4
 0.0045
P689 afflicts 6
 0.0044
P7807 ICD-11 (foundation) 44
 0.0043
P1748 NCI Thesaurus ID 37
 0.0040
P1060 pathogen transmission process 1
 0.0038
P699 Disease Ontology ID 38
 0.0036
P920 LEM ID 2
 0.0035
P2737 union of 1
 0.0031
P4317 GARD rare disease ID 14
 0.0027
P4229 ICD-10-CM 23
 0.0026
P672 MeSH tree code 36
 0.0022
P2892 UMLS CUI 51
 0.0021
P563 ICD-O 2
 0.0020
P3720 GPnotebook ID 1
 0.0020
P6363 WordLift URL 3
 0.0019
P9084 ABC News topic ID 2
 0.0018
P5270 MonDO ID 30
 0.0017
P1550 Orphanet ID 16
 0.0017