As of 2022-03-07, the Wikidata property age of onset (P2841) is used on 6 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
P2892 UMLS CUI 6
0.0002
P279 subclass of 6
0.0000
P2888 exact match 5
0.0000
P4229 ICD-10-CM 4
0.0005
P1748 NCI Thesaurus ID 4
0.0004
P7807 ICD-11 (foundation) 4
0.0004
P699 Disease Ontology ID 4
0.0004
P5270 MonDO ID 4
0.0002
P486 MeSH descriptor ID 4
0.0001
P5008 on focus list of Wikimedia project 4
0.0000
P7995 NHS Health A to Z ID 3
0.0055
P1461 Patientplus ID 3
0.0040
P780 symptoms and signs 3
0.0017
P604 MedlinePlus ID 3
0.0015
P673 eMedicine ID 3
0.0011
P557 DiseasesDB 3
0.0010
P1692 ICD-9-CM 3
0.0007
P7329 ID (MMS) 3
0.0004
P1995 health specialty 3
0.0004
P672 MeSH tree code 3
0.0002
P492 OMIM ID 3
0.0001
P3827 JSTOR topic ID 3
0.0001
P1417 Encyclopædia Britannica Online ID 3
0.0000
P373 Commons category 3
0.0000
P18 image 3
0.0000
P646 Freebase ID 3
0.0000
P31 instance of 3
0.0000
P1193 prevalence 2
0.0217
P924 possible treatment 2
0.0064
P7464 Genetics Home Reference Conditions ID 2
0.0026
P667 ICPC 2 ID 2
0.0021
P3841 Human Phenotype Ontology ID 2
0.0011
P5082 Store medisinske leksikon ID 2
0.0007
P493 ICD-9 2
0.0005
P2004 NALT ID 2
0.0003
P828 has cause 2
0.0003
P2293 genetic association 2
0.0003
P1550 Orphanet ID 2
0.0002
P665 KEGG ID 2
0.0001
P2347 YSO ID 2
0.0001
P8408 KBpedia ID 2
0.0001
P10283 OpenAlex ID 2
0.0000
P8189 National Library of Israel J9U ID 2
0.0000
P3417 Quora topic ID 2
0.0000
P1343 described by source 2
0.0000
P227 GND ID 2
0.0000
P244 Library of Congress authority ID 2
0.0000
P2074 internetmedicin.se ID 1
0.0152
P5642 risk factor 1
0.0081
P1479 has contributing factor 1
0.0032

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P1193 prevalence 2
0.0217
P2074 internetmedicin.se ID 1
0.0152
P5642 risk factor 1
0.0081
P924 possible treatment 2
0.0064
P7995 NHS Health A to Z ID 3
0.0055
P1461 Patientplus ID 3
0.0040
P1479 has contributing factor 1
0.0032
P923 medical examinations 1
0.0030
P7464 Genetics Home Reference Conditions ID 2
0.0026
P667 ICPC 2 ID 2
0.0021
P780 symptoms and signs 3
0.0017
P604 MedlinePlus ID 3
0.0015
P8656 Symptom Ontology ID 1
0.0012
P673 eMedicine ID 3
0.0011
P3841 Human Phenotype Ontology ID 2
0.0011
P557 DiseasesDB 3
0.0010
P2176 drug or therapy used for treatment 1
0.0008
P689 afflicts 1
0.0008
P1692 ICD-9-CM 3
0.0007
P5082 Store medisinske leksikon ID 2
0.0007
P6363 WordLift URL 1
0.0006
P493 ICD-9 2
0.0005
P4229 ICD-10-CM 4
0.0005
P1748 NCI Thesaurus ID 4
0.0004
P3471 WikiSkripta ID 1
0.0004
P7807 ICD-11 (foundation) 4
0.0004
P7329 ID (MMS) 3
0.0004
P699 Disease Ontology ID 4
0.0004
P1995 health specialty 3
0.0004
P2004 NALT ID 2
0.0003
P828 has cause 2
0.0003
P2293 genetic association 2
0.0003
P2892 UMLS CUI 6
0.0002
P5270 MonDO ID 4
0.0002
P1550 Orphanet ID 2
0.0002
P6058 Larousse ID 1
0.0002
P4317 GARD rare disease ID 1
0.0002
P3569 Cultureel Woordenboek ID 1
0.0002
P672 MeSH tree code 3
0.0002
P10 video 1
0.0002
P492 OMIM ID 3
0.0001
P3827 JSTOR topic ID 3
0.0001
P7033 Australian Educational Vocabulary ID 1
0.0001
P486 MeSH descriptor ID 4
0.0001
P665 KEGG ID 2
0.0001
P3984 subreddit 1
0.0001
P1245 OmegaWiki Defined Meaning 1
0.0001
P2347 YSO ID 2
0.0001
P2959 permanent duplicated item 1
0.0001
P3553 Zhihu topic ID 1
0.0001