User:Magnus Manske/Mix'n'match report/668

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.
• 'External ID' refers to the IDs in the original (external) catalog; the same as the statement value for the associated property.

MeSH Named Groups

Medical Subject Headings for Named Groups

Unknown external ID

• 401 external IDs in Wikidata but not in Mix'n'Match. Too many to show individually.

Different items for the same external ID

External ID	External label	Item in Wikidata	Item in Mix'n'Match	Mix'n'match entry
D000066792	Orthodontists	orthodontist (Q3842067)	118301}}	25738316
D000066794	Oral and Maxillofacial Surgeons	oral and maxillofacial surgeon (Q6041367)	504033}}	25738245
D000066989	Vegans	vegan (Q27522900)	181138}}	25738150
D000070777	School Teachers	school teacher (Q2251335)	37226}}	25738317
D000071195	Educational Personnel	educational personnel (Q93918935)	37226}}	25738324
D000071296	Government Employees	government employee (Q3796928)	212238}}	25738268
D000071959	Case Managers	case manager (Q70359971)	861362}}	25738221
D000072077	Anesthetists	anesthetist (Q2849224)	28837}}	25738179
D000072085	Dermatologists	dermatologist (Q2447386)	171171}}	25738087
D000072096	Cardiologists	cardiologist (Q3264451)	10379}}	25738355
D000072097	Endocrinologists	endocrinologist (Q4531850)	162606}}	25738107
D000072102	Gastroenterologists	gastroenterologist (Q19280221)	120569}}	25738231
D000072103	Oncologists	oncologist (Q16062369)	162555}}	25738235
D000072104	Nephrologists	nephrologist (Q20739489)	177635}}	25738302
D000072106	Pulmonologists	pulmonologist (Q24017632)	203337}}	25738156
D000072218	Endodontists	endodontist (Q67502614)	852143}}	25738194
D000072220	Otolaryngologists	otolaryngologist (Q2854916)	189553}}	25738353
D000072222	Nurses, Pediatric	pediatric nurse (Q69962711)	1741837}}	25738176
D000072339	Sexual Minorities	LGBT (Q17884)	589656}}	25738209
D001782	Blood Donors	blood donor (Q41311803)	53467}}	25738337
D006703	Homeless Persons	homeless person (Q29325697)	131327}}	25738229
D007198	Indians, North American	indigenous peoples of North America (Q15571255)	36747}}	25738152
D007230	Infant, Low Birth Weight	low birth weight infant (Q6692979)	1298973}}	25738220
D007231	Infant, Newborn	neonate (Q576104)	998}}	25738250
D007234	Infant, Premature	preterm infant (Q45051448)	625506}}	25738336
D009721	Nurse Midwives	nurse midwife (Q85790021)	185196}}	25738314
D010045	Outpatients	outpatient (Q67147922)	16962280}}	25738204
D010821	Physicians, Family	family physician (Q65472776)	3505712}}	25738132
D010822	Physicians, Women	woman physician (Q110228881)	8031527}}	25738252
D014171	Transients and Migrants	transient and migrant people (Q97322761)	128393}}	25738339
D016330	Frail Elderly	frail elderly (Q65619793)	177171}}	25738202
D018585	Battered Women	abused woman (Q105103095)	1800556}}	25738330
D019987	Visually Impaired Persons	person with visual disabilities (Q16649002)	737460}}	25738321
D033241	Lawyers	lawyer (Q40348)	6802429}}	25738247
D040441	Health Educators	health educator (Q64025283)	60894}}	25738154
D044382	Population Groups	population group (Q851990)	16334295}}	25738238
D052577	Infant, Extremely Low Birth Weight	extremely low birth weight infant (Q67579753)	6692979}}	25738187
D055815	Young Adult	young adult (Q17156455)	185193}}	25738228
D057229	Alcoholics	alcoholic (Q9148481)	15326}}	25738346
D064689	Nurses, Public Health	public health nurse (Q67529900)	7257749}}	25738111

Same item for multiple external IDs in Mix'n'match

Item in Mix'n'Match	Mix'n'match entry	External ID	External label
infant (Q998)	25738250	D007231	Infant, Newborn
	25738276	D007223	Infant
anesthesiologist (Q28837)	25738138	D000072080	Anesthesiologists
	25738179	D000072077	Anesthetists
teacher (Q37226)	25738317	D000070777	School Teachers
	25738324	D000071195	Educational Personnel
small for gestational age (Q1298973)	25738220	D007230	Infant, Low Birth Weight
	25738351	D007236	Infant, Small for Gestational Age

Multiple items for the same external ID in Wikidata

External ID	Items in Mix'n'Match
C016766	(+/-)-sulforaphane (Q424489) (R)-sulforaphane (Q27120804)
C023665	(−)-cathinone (Q414242) cathinone (Q7632116)
C027576	4-hydroxy-2-nonenal (Q229982) 4-hydroxynonenal (Q74428599)
C031233	Polyhexanide (Q408205) 1-(diaminomethylidene)-2-hexylguanidine (Q114905732)
C041376	rosmarinic acid (Q7762) (R)-rosmarinic acid (Q50380051)
C535289	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (Q940210) Rapp-Hodgkin syndrome (Q7294342)
C535351	cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome (Q55345761) autosomal dominant optic atrophy plus syndrome (Q55345901)
C535358	choroidal sclerosis (Q18558226) central areolar choroidal dystrophy (Q55345702)
C535380	X-linked spinal muscular atrophy type 2 (Q8041562) infantile-onset X-linked spinal muscular atrophy (Q55345741)
C535444	alpha-methylacyl-CoA racemase deficiency (Q27164415) congenital bile acid synthesis defect 4 (Q42863600)
C535504	autosomal recessive multiple epiphyseal dysplasia (Q3042144) autosomal recessive multiple epiphyseal dysplasia (Q60195170)
C535523	infantile onset spinocerebellar ataxia (Q18553306) mitochondrial DNA depletion syndrome 7 (Q26492819)
C535564	hypoplastic tibiae-postaxial polydactyly syndrome (Q17122962) absent tibia-polydactyly syndrome (Q56014402)
C535576	Heart valve dysplasia (Q5692507) X-linked cardiac valvular dysplasia (Q102293803)
C535761	familial nephrotic syndrome (Q2160802) nephrotic syndrome type 1 (Q61913400)
C535952	eosinophilic gastritis (Q18556159) eosinophilic gastroenteritis (Q27555722)
C536085	Ichthyosis follicularis with alopecia and photophobia syndrome (Q5986440) ichthyosis follicularis-alopecia-photophobia syndrome 1 (Q102293700)
C536189	ectrodactyly–ectodermal dysplasia–cleft syndrome (Q5334319) ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 (Q28065588) ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1 (Q28065589)
C536209	congenital central hypoventilation syndrome (Q979129) Haddad syndrome (Q56014441)
C536214	cold-induced sweating syndrome (Q3961672) Crisponi syndrome (Q55998740)
C536252	metaphyseal dysplasia (Q13566985) Metaphyseal dysplasia, Pyle type (Q22965556)
C536281	pulmonary hemosiderosis (Q1052626) Alveolar hypoventilation syndrome (Q64425127)
C536350	mitochondrial DNA depletion syndrome 1 (Q6881876) mitochondrial DNA depletion syndrome 8a (Q26492820) oculogastrointestinal muscular dystrophy (Q55782392) mitochondrial DNA depletion syndrome 8b (Q63859996)
C536364	hereditary neurocutaneous malformation (Q55780322) Hereditary neurocutaneous angioma (Q114044181)
C536377	nonsyndromic congenital nail disorder 4 (Q18553374) anonychia congenita (Q22443772)
C536522	X-linked myopathy with excessive autophagy (Q3456637) Autophagic vacuolar myopathy (Q63874868)
C536535	venous aneurysm (Q5676399) Vein of Galen aneurysmal malformations (Q11766796)
C536664	Zellweger spectrum disorder (Q51250082) peroxisomal biogenesis disorder (Q61913385)
C536868	hereditary spastic paraplegia 9A (Q32143434) autosomal dominant spastic paraplegia type 9 (Q55345928)
C536943	tarsal-carpal coalition syndrome (Q18553474) calcaneonavicular coalition (Q18554815)
C537206	spinocerebellar ataxia type 29 (Q21097773) spinocerebellar ataxia type 30 (Q21097774)
C537240	progressive supranuclear palsy-parkinsonism syndrome (Q55345717) atypical progressive supranuclear palsy syndrome (Q55346109)
C537436	Aromatase deficiency (Q4795506) aromatase excess syndrome (Q4795508)
C537492	Stickler syndrome (Q2288646) Stickler syndrome type 1 (Q55345651)
C537724	Lujan–Fryns syndrome (Q640836) syndromic X-linked intellectual disability 14 (Q28065625)
C537743	Oguchi disease-1 (Q7080278) congenital stationary night blindness (Q18553290) hereditary night blindness (Q18557952)
C538090	surface epithelial-stromal tumor (Q7645976) ovarian carcinoma (Q18556145)
C538125	alopecia macular degeneration growth retardation syndrome (Q56014555) Kuster Majewski Hammerstein syndrome (Q56014598)
C538187	Acrogeria (Q4675775) metageria (Q6822520)
C538208	Familial British dementia (Q5432926) ABri amyloidosis (Q50349602)
C538388	X-linked hypertrichosis (Q8041556) X-linked congenital generalized hypertrichosis (Q55345748)
C538618	paroxysmal cold hemoglobinuria (Q734042) Donath–Landsteiner hemolytic anemia (Q65120981)
C562924	Dowling-Degos disease (Q7316720) reticulate acropigmentation of Kitamura (Q7316721)
C563020	anal canal carcinoma (Q2652259) cloacogenic carcinoma (Q18557499)
C563162	familial calcium pyrophosphate deposition (Q55950198) calcium pyrophosphate dihydrate crystal deposition disease (Q64348505)
C563835	drug metabolism, poor, Cyp2D6-related (Q55783616) Poor drug metabolism (Q109905255)
C564525	GATA 1 related cytopenia (Q3009546) thrombocytopenia with congenital dyserythropoietic anemia (Q56014250)
C565089	calvarial doughnut lesions-bone fragility syndrome (Q55780509) calvarial doughnut lesions-bone fragility syndrome (Q102293214)
C565535	granulocytopenia with immunoglobulin abnormality (Q55781920) immunodeficiency 59 (Q102294307)
C565637	deafness, sensorineural, autosomal-mitochondrial type (Q55781811) autosomal-mitochondrial sensorineural deafness (Q102293457)
C566897	Ligneous conjunctivitis (Q6546687) plasminogen deficiency type I (Q97109018)
C566917	Glycogen storage disease type 0 (Q5572606) glycogen storage disease type 0B (Q109676512)
C574275	ectrodactyly (Q650026) 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)
C580039	mitochondrial DNA depletion syndrome 3 (Q26492815) mitochondrial DNA depletion syndrome, hepatocerebral form (Q55786491)
C580174	Huntington's disease-like syndrome (Q24977062) Huntington disease and related disorders (Q55345637)
C580473	mitochondrial DNA depletion syndrome 5 (Q26492817) mitochondrial DNA depletion syndrome 9 (Q26492821)
D000083682	opioid overdose (Q17154378) opioid overdose (Q30100108)
D001714	bipolar disorder (Q131755) bipolar I disorder (Q4915474)
D001921	brain (Q1073) human brain (Q492038)
D002543	cerebral hemorrhage (Q1368943) hereditary cystatin C amyloid angiopathy (Q10992004)
D002583	cervix uterine cancer (Q160105) uterine cervix neoplasm (Q56014502)
D002613	cheilitis (Q1068997) cheilitis exfoliativa (Q1343695)
D003486	cyanide poisoning (Q883082) cyanide (Q55076544)
D003607	dacryocystitis (Q1157761) dacryoadenitis (Q1424488)
D003711	demyelination (Q1186697) demyelinating disease (Q1186703)
D003924	maturity-onset diabetes of the young (Q663041) type 2 diabetes (Q3025883)
D004242	diving (Q7735) underwater diving (Q179643)
D004326	drinking (Q876776) water consumption (Q1277412)
D004401	dysarthria (Q225957) scanning speech (Q7430080)
D004480	ectromelia (Q1323724) fibular hemimelia (Q1411024)
D004541	Eisenmenger's syndrome (Q572695) Eisenmenger complex (Q1313103)
D004938	esophageal cancer (Q372701) esophageal neoplasm (Q56014520)
D005525	food manufacturer (Q1252971) food manufacturing (Q2836940)
D005538	American football (Q41323) football codes (Q1081491)
D005715	gambling (Q11416) problem gambling (Q748309)
D005820	genetic testing (Q285223) genetic screen (Q5050812)
D006001	glycoconjugate (Q416019) glycoconjugates [Golgi lumen] (Q50268135)
D006111	toxic diffuse goiter (Q16483) Graves' disease (Q50357588)
D006223	Cowden syndrome 1 (Q1138188) Lhermitte–Duclos disease (Q1461101) multiple hamartoma syndrome (Q3508737)
D006257	head (Q23640) human head (Q3409626)
D006321	heart (Q1072) human heart (Q2419844)
D006394	hemangiosarcoma (Q539728) angiosarcoma (Q2619091)
D006841	aromatic compound (Q19834818) NIOSH Method 1501: Hydrocarbons, Aromatic (Q21761549)
D006967	allergy (Q42982) pet dander allergy (Q5481761) hypersensitivity (Q5958765)
D007174	kleptomania (Q212021) impulse control disorder (Q1201835)
D007822	laryngeal cancer (Q852423) laryngeal neoplasm (Q18555128)
D007889	uterine fibroid (Q556281) leiomyoma (Q4667534)
D008103	liver cirrhosis (Q147778) cirrosis (Q12569389)
D008168	lung (Q7886) human lung (Q2640512)
D008199	adenitis (Q355981) lymphadenitis (Q3269466)
D008209	lymphedema (Q916398) hereditary lymphedema (Q1996246)
D008268	age related macular degeneration (Q830308) macular degeneration (Q27429789)
D008334	mandible (Q16370) human mandible (Q5283631)
D008548	freckle (Q187882) melanosis (Q6811539)
D008607	intellectual disability (Q183560) imbecile (Q4200185)
D009055	mouth (Q9635) human mouth (Q1370895)
D009221	fibrodysplasia ossificans progressiva (Q1410831) myositis ossificans (Q3858675)
D009369	cancer (Q12078) neoplasm (Q1216998)
D009477	congenital insensitivity to pain with anhidrosis (Q501694) hereditary sensory and autonomic neuropathy (Q3702898)
D009666	nose (Q7363) human nose (Q2673594)
D009765	obesity (Q12174) epidemiology of obesity (Q5382727)
D010000	bone inflammation disease (Q1178507) Osteítis (Q21141385)
D010002	osteitis fibrosa cystica (Q799615) brown tumor (Q4976425)
D010009	multiple epiphyseal dysplasia (Q1452604) osteochondrodysplasia (Q3251367)
D010031	otitis (Q480700) Infectious otitis in animals (Q6054536)
D010051	ovarian cancer (Q172341) ovarian neoplasm (Q11793790)
D010190	pancreatic cancer (Q212961) pancreatic neoplasm (Q7130412)
D010259	delusional disorder (Q721073) paranoia (Q1229994)
D010282	parathyroid carcinoma (Q40301) parathyroid neoplasm (Q7136148)
D010373	Pediculus humanus capitis infestation (Q532158) lice infestation (Q1343674)
D010412	penile cancer (Q1342955) penile neoplasm (Q18554121)
D010554	personality disorder (Q270673) avoidant personality disorder (Q509122) narcissistic personality disorder (Q1060310)
D010731	phosphoenolpyruvate-dependent sugar phosphotransferase system (Q21199241) PTS-GFL superfamily (Q25112332) PTS-AG superfamily (Q28209150)
D010854	black piedra (Q2059411) piedra (Q10863066)
D011009	pneumoconiosis (Q651223) bagassosis (Q4841462)
D011014	pneumonia (Q12192) pneumonitis (Q1284347)
D011502	marasmus (Q582904) protein-energy malnutrition (Q4082071)
D011618	psychosis (Q170082) schizoaffective disorder (Q834047) schizophreniform disorder (Q2157462)
D011695	Henoch-Schoenlein purpura (Q1035319) Henoch-Schönlein nephritis (Q16611043)
D011906	sodoku (Q1807401) rat-bite fever (Q2754970)
D012131	respiratory failure (Q767485) acute respiratory insufficiency (Q21006662)
D012170	central retinal vein occlusion (Q190831) retinal vein occlusion (Q18554884)
D012734	pseudohermaphroditism (Q2273662) disorder of sex development (Q5282521)
D012772	toxic shock syndrome (Q1128440) septic shock (Q1765564)
D012867	skin (Q1074) human skin (Q5259911)
D012886	human skull (Q9604) skull (Q13147)
D012893	sleep disorder (Q177190) sleep-wake disorder (Q54972453)
D013274	stomach cancer (Q189588) stomach neoplasm (Q4335552)
D013502	general surgery (Q932510) history of surgery (Q2556088)
D013734	androgen insensitivity syndrome (Q512313) Estrogen insensitivity syndrome (Q5401847)
D013736	testicular cancer (Q324464) tumor of testis and paratestis (Q55787784)
D013964	thyroid cancer (Q826522) thyroid neoplasm (Q13632630)
D013991	Tietze syndrome (Q175763) costochondritis (Q5175170)
D014211	bejel (Q682798) treponematosis (Q1243869)
D014314	trisomy (Q844903) Warkany syndrome (Q2454191)
D014347	Trypanosoma brucei gambiense (Q9396337) Trypanosoma brucei gambiense (Q30216048)
D014438	typhus (Q160649) epidemic typhus (Q1290616)
D014594	uterine cancer (Q1209744) uterine neoplasm (Q56014517)
D014689	chronic cerebrospinal venous insufficiency (Q1088054) venous insufficiency (Q9008818)
D014714	Vertebrata (Q25241) vertebrate (Q110551902)
D014754	violence (Q124490) violence prevention (Q104733130)
D014897	spinal muscular atrophy (Q580290) juvenile spinal muscular atrophy (Q18554312)
D015451	chronic lymphocytic leukemia (Q1088156) small lymphocytic lymphoma (Q9022766)
D015675	Bone gamma-carboxyglutamate protein (Q415863) osteocalcin (Q59250722)
D016464	lysosomal storage disease (Q675010) Q16562088
D016472	lateral sclerosis (Q2881413) motor neuron disease (Q3221083)
D016906	Interleukin 9 (Q2563463) Interleukin-9 (Q24787897)
D017129	anisakiasis (Q3091959) anisakidosis (Q48782762)
D018249	oxyphilic adenoma (Q1760202) Hurthle cell (Q4223446)
D018270	invasive ductal carcinoma (Q1671685) breast ductal carcinoma (Q3658404)
D018332	Spitz nevus (Q2311457) epithelioid and spindle cell nevus (Q18971640)
D019556	COS cell line (Q5013524) COS-7 (Q27556092)
D020921	sleep sex (Q1637663) sleep arousal disorder (Q19001302)
D026724	ethical review (Q56515249) medical ethical review (Q59094171)
D029461	Salla disease (Q3843807) sialuria (Q7506696)
D044464	F2R like trypsin receptor 1 (Q21115613) protease-activated receptor 2 (Q24722679)
D046110	gestational hypertension (Q1519482) hypertensive disease of pregnancy (Q19001368)
D050090	true hermaphroditism (Q7847568) ovotesticular disorder of sex development (Q54944059)
D050644	Succinate-semialdehyde dehydrogenase (NAD+) (Q3976579) Succinate-semialdehyde dehydrogenase (NAD(P)+) (Q3976581)
D051379	Mus (Q39275) mouse (Q2751034)
D053450	TNF receptor superfamily member 18 (Q21135817) tumor necrosis factor receptor 18 (Q24784554)
D054380	C-X-C motif chemokine receptor 5 (Q1024612) CXC chemokine receptor 5 (Q24727201)
D056587	Muckle-Wells syndrome (Q1538218) cryopyrin-associated periodic syndrome (Q1771331) familial cold urticaria (Q1835481)
D057809	HEK293 (Q489618) HEK293T (Q27546876)
D058531	XX male syndrome (Q365589) XX male syndrome (Q28401082)
D064028	Tracheophyta (Q27133) conifer (Q132825)
D064193	Anaphase promoting complex subunit 5 (Q21130504) anaphase-promoting complex subunit 5 (Q54438951)
D066194	rhinencephalon (Q1153195) olfactory cortex (Q70750040)