As of 2022-03-07, the Wikidata property NHS Health A to Z ID (P7995) is used on 541 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 523
0.0002
P646 Freebase ID 481
0.0001
P1995 health specialty 461
0.0540
P486 MeSH descriptor ID 456
0.0123
P10283 OpenAlex ID 449
0.0045
P373 Commons category 446
0.0001
P672 MeSH tree code 437
0.0264
P2892 UMLS CUI 436
0.0176
P2888 exact match 435
0.0001
P3827 JSTOR topic ID 404
0.0159
P7807 ICD-11 (foundation) 402
0.0384
P557 DiseasesDB 397
0.1260
P5008 on focus list of Wikimedia project 397
0.0006
P604 MedlinePlus ID 382
0.1784
P1417 Encyclopædia Britannica Online ID 382
0.0022
P673 eMedicine ID 378
0.1355
P699 Disease Ontology ID 371
0.0345
P18 image 371
0.0001
P7329 ID (MMS) 358
0.0442
P1748 NCI Thesaurus ID 347
0.0364
P3417 Quora topic ID 346
0.0019
P5270 MonDO ID 314
0.0177
P4229 ICD-10-CM 313
0.0346
P244 Library of Congress authority ID 300
0.0002
P31 instance of 295
0.0000
P1692 ICD-9-CM 292
0.0663
P508 BNCF Thesaurus ID 285
0.0172
P8189 National Library of Israel J9U ID 265
0.0015
P5082 Store medisinske leksikon ID 253
0.0780
P8408 KBpedia ID 252
0.0066
P1461 Patientplus ID 251
0.2402
P6366 Microsoft Academic ID 249
0.0009
P2347 YSO ID 244
0.0101
P2176 drug or therapy used for treatment 243
0.1523
P3471 WikiSkripta ID 219
0.0825
P268 Bibliothèque nationale de France ID 216
0.0004
P493 ICD-9 212
0.0497
P227 GND ID 211
0.0002
P667 ICPC 2 ID 209
0.1643
P494 ICD-10 209
0.0427
P665 KEGG ID 202
0.0099
P4527 UK Parliament thesaurus ID 200
0.0076
P910 topic's main category 200
0.0003
P4317 GARD rare disease ID 193
0.0356
P3841 Human Phenotype Ontology ID 192
0.0901
P349 National Diet Library ID 187
0.0013
P1296 Gran Enciclopèdia Catalana ID 182
0.0016
P492 OMIM ID 180
0.0073
P3219 Encyclopædia Universalis ID 173
0.0052
P1550 Orphanet ID 167
0.0171

Closest properties by Jaccard index

IDLabelIntersection cardinalityJaccard index
P1461 Patientplus ID 251
0.2402
P604 MedlinePlus ID 382
0.1784
P667 ICPC 2 ID 209
0.1643
P2176 drug or therapy used for treatment 243
0.1523
P673 eMedicine ID 378
0.1355
P557 DiseasesDB 397
0.1260
P924 possible treatment 74
0.0956
P3841 Human Phenotype Ontology ID 192
0.0901
P923 medical examinations 70
0.0875
P3471 WikiSkripta ID 219
0.0825
P5082 Store medisinske leksikon ID 253
0.0780
P780 symptoms and signs 158
0.0744
P7464 Genetics Home Reference Conditions ID 83
0.0680
P1692 ICD-9-CM 292
0.0663
P5806 SNOMED CT identifier 76
0.0595
P1995 health specialty 461
0.0540
P2074 internetmedicin.se ID 29
0.0506
P493 ICD-9 212
0.0497
P1193 prevalence 29
0.0483
P1060 pathogen transmission process 34
0.0480
P8656 Symptom Ontology ID 62
0.0472
P3487 maximal incubation period in humans 29
0.0463
P3488 minimal incubation period in humans 29
0.0462
P7329 ID (MMS) 358
0.0442
P494 ICD-10 209
0.0427
P5642 risk factor 26
0.0411
P7807 ICD-11 (foundation) 402
0.0384
P1748 NCI Thesaurus ID 347
0.0364
P4317 GARD rare disease ID 193
0.0356
P4229 ICD-10-CM 313
0.0346
P699 Disease Ontology ID 371
0.0345
P6363 WordLift URL 68
0.0334
P668 GeneReviews ID 20
0.0298
P9084 ABC News topic ID 44
0.0286
P672 MeSH tree code 437
0.0264
P1583 MalaCards ID 15
0.0263
P1605 has natural reservoir 15
0.0231
P920 LEM ID 22
0.0215
P9272 DeCS ID 45
0.0204
P2004 NALT ID 138
0.0197
P3569 Cultureel Woordenboek ID 109
0.0192
P5131 possible medical findings 11
0.0185
P2854 disease burden 10
0.0183
P2293 genetic association 146
0.0179
P5270 MonDO ID 314
0.0177
P2892 UMLS CUI 436
0.0176
P689 afflicts 32
0.0175
P508 BNCF Thesaurus ID 285
0.0172
P1550 Orphanet ID 167
0.0171
P3827 JSTOR topic ID 404
0.0159