Wikidata

User:Magnus Manske/Mix'n'match report/666

< User:Magnus Manske‎ | Mix'n'match report

A report for the Mix'n'match tool. This page will be replaced regularly! Please note: If you fix something from this list on Wikidata, please fix it on Mix'n'match as well, if applicable. Otherwise, the error might be re-introduced from there.

MeSH Humanities edit

Medical Subject Headings for Humanities

Unknown external ID edit

  • 46801 entries for this, not showing

Mismatch between Wikidata and Mix'n'match edit

  1. Wikidata says the external ID D000716 belongs to artistic anatomy (Q1213552), but mix'n'match says artistic anatomy (Q6103502)
  2. Wikidata says the external ID D017041 belongs to ethics committee (Q59057226), but mix'n'match says medical ethics committee (Q27913684)
  3. Wikidata says the external ID D028743 belongs to professional misconduct (Q64831582), but mix'n'match says malpractice (Q318836)
  4. Wikidata says the external ID D008513 belongs to medicine in literature (Q65587654), but mix'n'match says medical fiction (Q20664427)
  5. Wikidata says the external ID D026684 belongs to personal autonomy (Q67376917), but mix'n'match says Personal autonomy (Q19927678)
  6. Wikidata says the external ID D005789 belongs to genealogy and heraldry (Q97577059), but mix'n'match says genealogy (Q47307)

Multiple items with same external ID edit

  1. Multiple Wikidata items with external ID C565089 : calvarial doughnut lesions-bone fragility syndrome (Q102293214), calvarial doughnut lesions-bone fragility syndrome (Q55780509)
  2. Multiple Wikidata items with external ID C565637 : autosomal-mitochondrial sensorineural deafness (Q102293457), deafness, sensorineural, autosomal-mitochondrial type (Q55781811)
  3. Multiple Wikidata items with external ID C536085 : ichthyosis follicularis-alopecia-photophobia syndrome 1 (Q102293700), Ichthyosis follicularis with alopecia and photophobia syndrome (Q5986440)
  4. Multiple Wikidata items with external ID C535576 : X-linked cardiac valvular dysplasia (Q102293803), Heart valve dysplasia (Q5692507)
  5. Multiple Wikidata items with external ID C565476 : hypoproteinemia, Hypercatabolic (Q102293947), hypoproteinemia, Hypercatabolic (Q55781980)
  6. Multiple Wikidata items with external ID C565535 : immunodeficiency 59 (Q102294307), granulocytopenia with immunoglobulin abnormality (Q55781920)
  7. Multiple Wikidata items with external ID D014754 : violence prevention (Q104733130), violence (Q124490)
  8. Multiple Wikidata items with external ID D000086382 : COVID-19 mortality (Q104778232), COVID-19 (Q84263196)
  9. Multiple Wikidata items with external ID C536281 : pulmonary hemosiderosis (Q1052626), Alveolar hypoventilation syndrome (Q64425127)
  10. Multiple Wikidata items with external ID D013060 : speech physiology (Q105549868), speech (Q52946)
  11. Multiple Wikidata items with external ID D003331 : myocardial blood supply (Q106120773), coronary vessel (Q67315798)
  12. Multiple Wikidata items with external ID C566917 : glycogen storage disease type 0B (Q109676512), Glycogen storage disease type 0 (Q5572606)
  13. Multiple Wikidata items with external ID D007117 : booster dose (Q109746711), booster dose (Q73213117)
  14. Multiple Wikidata items with external ID C563835 : Poor drug metabolism (Q109905255), drug metabolism, poor, Cyp2D6-related (Q55783616)
  15. Multiple Wikidata items with external ID D000072339 : gender minority (Q11894636), sexual minority (Q589656), LGBT (Q17884)
  16. Multiple Wikidata items with external ID D064028 : conifer (Q132825), conifer (Q69465975), Tracheobionta (Q69466161), Tracheophyta (Q27133)
  17. Multiple Wikidata items with external ID C536252 : metaphyseal dysplasia (Q13566985), Metaphyseal dysplasia, Pyle type (Q22965556)
  18. Multiple Wikidata items with external ID D009055 : human mouth (Q1370895), mouth (Q9635)
  19. Multiple Wikidata items with external ID C535564 : hypoplastic tibiae-postaxial polydactyly syndrome (Q17122962), absent tibia-polydactyly syndrome (Q56014402)
  20. Multiple Wikidata items with external ID D008607 : intellectual disability (Q183560), idiot (Q193607), imbecile (Q4200185)
  21. Multiple Wikidata items with external ID C537743 : congenital stationary night blindness (Q18553290), hereditary night blindness (Q18557952), Oguchi disease-1 (Q7080278)
  22. Multiple Wikidata items with external ID C535523 : infantile onset spinocerebellar ataxia (Q18553306), mitochondrial DNA depletion syndrome 7 (Q26492819)
  23. Multiple Wikidata items with external ID C536377 : nonsyndromic congenital nail disorder 4 (Q18553374), anonychia congenita (Q22443772)
  24. Multiple Wikidata items with external ID C536943 : tarsal-carpal coalition syndrome (Q18553474), calcaneonavicular coalition (Q18554815)
  25. Multiple Wikidata items with external ID C538090 : ovarian carcinoma (Q18556145), surface epithelial-stromal tumor (Q7645976)
  26. Multiple Wikidata items with external ID C535952 : eosinophilic gastritis (Q18556159), eosinophilic gastroenteritis (Q27555722)
  27. Multiple Wikidata items with external ID C563020 : cloacogenic carcinoma (Q18557499), anal canal carcinoma (Q2652259)
  28. Multiple Wikidata items with external ID C535358 : choroidal sclerosis (Q18558226), central areolar choroidal dystrophy (Q55345702)
  29. Multiple Wikidata items with external ID C537206 : spinocerebellar ataxia type 29 (Q21097773), spinocerebellar ataxia type 30 (Q21097774)
  30. Multiple Wikidata items with external ID C535761 : familial nephrotic syndrome (Q2160802), nephrotic syndrome type 1 (Q61913400)
  31. Multiple Wikidata items with external ID C537492 : Stickler syndrome (Q2288646), Stickler syndrome type 1 (Q55345651)
  32. Multiple Wikidata items with external ID D003861 : depersonalization disorder (Q2338307), depersonalization (Q83177)
  33. Multiple Wikidata items with external ID D006321 : human heart (Q2419844), heart (Q1072)
  34. Multiple Wikidata items with external ID D016906 : Interleukin-9 (Q24787897), Interleukin 9 (Q2563463)
  35. Multiple Wikidata items with external ID D061865 : hemorrhoidectomy (Q24961157), hemorrhoidectomy (Q73508269)
  36. Multiple Wikidata items with external ID C580174 : Huntington's disease-like syndrome (Q24977062), Huntington disease and related disorders (Q55345637)
  37. Multiple Wikidata items with external ID D013502 : history of surgery (Q2556088), general surgery (Q932510)
  38. Multiple Wikidata items with external ID D008168 : human lung (Q2640512), lung (Q7886)
  39. Multiple Wikidata items with external ID C580047 : DMD-related dilated cardiomyopathy (Q26492779), DMD-related dilated cardiomyopathy (Q28024586)
  40. Multiple Wikidata items with external ID C580039 : mitochondrial DNA depletion syndrome 3 (Q26492815), mitochondrial DNA depletion syndrome, hepatocerebral form (Q55786491)
  41. Multiple Wikidata items with external ID C580473 : mitochondrial DNA depletion syndrome 5 (Q26492817), mitochondrial DNA depletion syndrome 9 (Q26492821)
  42. Multiple Wikidata items with external ID C536350 : mitochondrial DNA depletion syndrome 8a (Q26492820), oculogastrointestinal muscular dystrophy (Q55782392), mitochondrial DNA depletion syndrome 8b (Q63859996), mitochondrial DNA depletion syndrome 1 (Q6881876)
  43. Multiple Wikidata items with external ID D009666 : human nose (Q2673594), nose (Q7363)
  44. Multiple Wikidata items with external ID C535444 : alpha-methylacyl-CoA racemase deficiency (Q27164415), congenital bile acid synthesis defect 4 (Q42863600)
  45. Multiple Wikidata items with external ID D051379 : mouse (Q2751034), Mus (Q39275)
  46. Multiple Wikidata items with external ID D057809 : HEK293T (Q27546876), HEK293 (Q489618)
  47. Multiple Wikidata items with external ID D019556 : COS-7 (Q27556092), COS cell line (Q5013524)
  48. Multiple Wikidata items with external ID C536189 : ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 (Q28065588), ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 (Q28065589), ectrodactyly–ectodermal dysplasia–cleft syndrome (Q5334319)
  49. Multiple Wikidata items with external ID C537724 : syndromic X-linked intellectual disability 14 (Q28065625), Lujan–Fryns syndrome (Q640836)
  50. Multiple Wikidata items with external ID D058531 : XX male syndrome (Q28401082), XX male syndrome (Q365589)
  51. Multiple Wikidata items with external ID D005820 : genetic testing (Q285223), genetic screen (Q5050812)
  52. Multiple Wikidata items with external ID C564525 : GATA 1 related cytopenia (Q3009546), thrombocytopenia with congenital dyserythropoietic anemia (Q56014250)
  53. Multiple Wikidata items with external ID D014347 : Trypanosoma brucei gambiense (Q30216048), Trypanosoma brucei gambiense (Q9396337)
  54. Multiple Wikidata items with external ID C535504 : autosomal recessive multiple epiphyseal dysplasia (Q3042144), autosomal recessive multiple epiphyseal dysplasia (Q60195170)
  55. Multiple Wikidata items with external ID C574275 : split hand-foot malformation (Q30989072), split hand-foot malformation 4 (Q30989218), split hand-foot malformation 5 (Q30989219), split hand-foot malformation 3 (Q42863539), split hand-foot malformation 2 (Q42863541), ectrodactyly (Q650026)
  56. Multiple Wikidata items with external ID C536868 : hereditary spastic paraplegia 9A (Q32143434), autosomal dominant spastic paraplegia type 9 (Q55345928)
  57. Multiple Wikidata items with external ID D006257 : human head (Q3409626), head (Q23640)
  58. Multiple Wikidata items with external ID C536522 : X-linked myopathy with excessive autophagy (Q3456637), Autophagic vacuolar myopathy (Q63874868)
  59. Multiple Wikidata items with external ID C536214 : cold-induced sweating syndrome (Q3961672), Crisponi syndrome (Q55998740)
  60. Multiple Wikidata items with external ID D050644 : Succinate-semialdehyde dehydrogenase (NAD+) (Q3976579), Succinate-semialdehyde dehydrogenase (NAD(P)+) (Q3976581)
  61. Multiple Wikidata items with external ID C538187 : Acrogeria (Q4675775), metageria (Q6822520)
  62. Multiple Wikidata items with external ID C537436 : Aromatase deficiency (Q4795506), aromatase excess syndrome (Q4795508)
  63. Multiple Wikidata items with external ID D001921 : human brain (Q492038), brain (Q1073)
  64. Multiple Wikidata items with external ID C538208 : ABri amyloidosis (Q50349602), Familial British dementia (Q5432926)
  65. Multiple Wikidata items with external ID C041376 : (R)-rosmarinic acid (Q50380051), rosmarinic acid (Q7762)
  66. Multiple Wikidata items with external ID C536664 : Zellweger spectrum disorder (Q51250082), peroxisomal biogenesis disorder (Q61913385)
  67. Multiple Wikidata items with external ID D012867 : human skin (Q5259911), skin (Q1074)
  68. Multiple Wikidata items with external ID D008334 : human mandible (Q5283631), mandible (Q16370)
  69. Multiple Wikidata items with external ID D025141 : antifungal drug resistance (Q53788821), antifungal drug resistance (Q70711118)
  70. Multiple Wikidata items with external ID D026141 : antifungal drug resistance (Q53788821), fungal multiple drug resistance (Q70695790)
  71. Multiple Wikidata items with external ID D009765 : epidemiology of obesity (Q5382727), obesity (Q12174)
  72. Multiple Wikidata items with external ID D003486 : cyanide (Q55076544), cyanide poisoning (Q883082)
  73. Multiple Wikidata items with external ID C537240 : progressive supranuclear palsy-parkinsonism syndrome (Q55345717), atypical progressive supranuclear palsy syndrome (Q55346109)
  74. Multiple Wikidata items with external ID C535380 : infantile-onset X-linked spinal muscular atrophy (Q55345741), X-linked spinal muscular atrophy type 2 (Q8041562)
  75. Multiple Wikidata items with external ID C538388 : X-linked congenital generalized hypertrichosis (Q55345748), X-linked hypertrichosis (Q8041556)
  76. Multiple Wikidata items with external ID C535351 : cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome (Q55345761), autosomal dominant optic atrophy plus syndrome (Q55345901)
  77. Multiple Wikidata items with external ID C563162 : familial calcium pyrophosphate deposition (Q55950198), calcium pyrophosphate dihydrate crystal deposition disease (Q64348505)
  78. Multiple Wikidata items with external ID C536209 : Haddad syndrome (Q56014441), congenital central hypoventilation syndrome (Q979129)
  79. Multiple Wikidata items with external ID C538125 : alopecia macular degeneration growth retardation syndrome (Q56014555), Kuster Majewski Hammerstein syndrome (Q56014598)
  80. Multiple Wikidata items with external ID D006967 : hypersensitivity (Q5958765), allergy (Q42982)
  81. Multiple Wikidata items with external ID C538618 : Donath–Landsteiner hemolytic anemia (Q65120981), paroxysmal cold hemoglobinuria (Q734042)
  82. Multiple Wikidata items with external ID D047494 : Peroxisome proliferator activated receptor delta (Q65162065), Peroxisome proliferator activated receptor delta (Q7169504)
  83. Multiple Wikidata items with external ID C566897 : Ligneous conjunctivitis (Q6546687), plasminogen deficiency type I (Q97109018)
  84. Multiple Wikidata items with external ID C535289 : Rapp-Hodgkin syndrome (Q7294342), ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (Q940210)
  85. Multiple Wikidata items with external ID C562924 : Dowling-Degos disease (Q7316720), reticulate acropigmentation of Kitamura (Q7316721)
  86. Multiple Wikidata items with external ID D012886 : skull (Q13147), human skull (Q9604)
Retrieved from "https://www.wikidata.org/w/index.php?title=User:Magnus_Manske/Mix%27n%27match_report/666&oldid=1541781200"