User:Magnus Manske/Mix'n'match report/633

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 Phenomena and Processes

MeSH Phenomena and Processes

Unknown external ID

• 35971 external IDs in Wikidata but not in Mix'n'Match. Too many to show individually.

Different items for the same external ID

External ID	Item in Wikidata	Item in Mix'n'Match	Mix'n'match entry
D012306	risk (Q104493)	risk assessment (Q1058438)	25395357
D000399	air pressure (Q67389075)	atmospheric pressure (Q81809)	25395533
D001827	human height (Q476112)	body height (Q2997702)	25396295
D059447	cell cycle checkpoint signaling (Q1068809)	Cell Cycle Checkpoints (Q36804385)	25395796
D001862	bone resorption (Q4941581)	bone resorption disease (Q18553741)	25394991
D020079	terminal repeat sequence (Q106580757)	long terminal repeat (Q1869477)	25394837
D009765	epidemiology of obesity (Q5382727)	obesity (Q12174)	25395614
D004352	antimicrobial resistance (Q63391344)	antibiotic resistance (Q380775)	25394655
D001947	breeding (Q65360845)	animal breeding (Q227675)	25394649
D005527	fortified food (Q66296884)	food fortification (Q15121266)	25394695
D013046	relative density (Q11027905)	relative density (Q10972285)	25396145
D014131	microelement (Q11781028)	trace metal (Q7831165)	25396547
D036801	birth (Q14819852)	parturition (Q34581)	25395937
D060434	herbivory (Q45874067)	herbivore (Q59099)	25396075
D002113	calcification (Q933382)	calcification (Q71159138)	25394815
D002873	chromosome fragility (Q71260880)	chromosomal fragile site (Q5113903)	25396441
D020567	fetal weight (Q67172386)	prenatal nutrition (Q7240527)	25394778
D055874	extreme heat (Q69044113)	heat wave (Q215864)	25396461
D040681	structural homology (Q62098098)	cell cycle (Q188941)	25394838
D014644	genetic variation (Q349856)	genetic diversity (Q585259)	25394931
D014314	trisomy (Q844903)	trisomy 9 (Q381719)	25394892
D014314	Warkany syndrome (Q2454191)	trisomy 9 (Q381719)	25394892
D040481	genome components (Q73351560)	DNA sequence (Q55579426)	25395858
D057141	preserved food (Q3687258)	food preservation (Q173514)	25395980
D004041	dietary fats (Q98879981)	fat (Q127980)	25396174
D055571	secretion (Q84230)	secretory pathway (Q7444453)	25396130
D011003	ploidy (Q118406)	HC Lada Togliatti (Q1349)	25394569
D041923	adolescence (Q131774)	Adolescent development (Q24556746)	25396207
D008598	menstruation (Q17155666)	menstruation (Q12171)	25396123
D015444	physical exercise (Q219067)	health enhancing physical activity (Q19710494)	25394581
D020022	genetic predisposition to disease (Q64843122)	genetic predisposition (Q784237)	25394633
D014110	touch (Q877674)	haptic perception (Q1289489)	25395046
D011270	pregnancy (Q1490716)	gestation (Q28627)	25395021
D050173	Y-linked gene (Q67200881)	Y linkage (Q2598585)	25395300
D012894	sleep stage (Q2237998)	sleep (Q35831)	25394707
D015394	molecular structure (Q100682626)	molecular geometry (Q911331)	25396099
D018919	physiologic neovascularization (Q105299511)	angiogenesis (Q539568)	25396223
D019680	trinucleotide repeat expansion (Q6736610)	trinucleotide repeat disorder (Q356736)	25395520
D011275	unwanted pregnancy (Q67359903)	unplanned pregnancy (Q3817591)	25395155
D003227	conjugation (Q22290285)	bacterial conjugation (Q273193)	25394469
D004042	unsaturated dietary fats (Q98881306)	unsaturated fat (Q652555)	25396231
D018965	ribosomal frameshifting (Q101830413)	viral translational frameshifting (Q22283375)	25395002
D005541	forced expiratory volume (Q102196648)	decreased forced expiratory volume (Q21110105)	25395008
D057131	evasion of host immune response (Q1660157)	response to defenses of other organism (Q22273865)	25395175
D014675	vegetable (Q11004)	Vegetables (Q1413783)	25396626
D018533	biomass (Q2945560)	biomass (Q18537)	25396349
D053580	muscle strength (Q3076906)	physical strength (Q1785966)	25396321
D006790	host-parasite interaction (Q65517745)	host-pathogen interaction (Q5909198)	25394535
D000067075	vegetable products (Q66684759)	vegetable (Q11004)	25396398
D016922	cellular senescence (Q9075999)	cell aging (Q14818028)	25396093
D003081	cold weather (Q23759587)	polar climate (Q193372)	25394810
D057885	Triploid syndrome (Q56137331)	triploidy (Q504558)	25395835
D058067	wavelet analysis (Q98815349)	wavelet transform (Q2867)	25396514
D044127	genetic epigenesis (Q64443099)	epigenesis (Q10273301)	25396142
D050259	mitochondrial gene (Q64829650)	mitochondrial DNA (Q27075)	25396149
D038301	virus inactivation (Q67506291)	inactivated vaccine (Q3560939)	25395446
D001772	blood cell count (Q48633601)	complete blood count (Q886518)	25394771
D005426	animal flight (Q89576883)	flying or gliding animal (Q2917486)	25394664
D017440	daylight cycle (Q106636923)	photoperiodism (Q259028)	25394556
D002877	human chromosomes (Q21169665)	Chromosomes, Human (Q1056398)	25395794
D004326	water consumption (Q1277412)	drinking (Q876776)	25395525
D020131	duplicate genes (Q100685808)	gene duplication (Q746284)	25395859
D064307	microbiota (Q104117645)	microbiome (Q1330402)	25394801
D065588	nasal absorption (Q66133422)	nasal administration (Q6966562)	25394841
D059786	abnormal karyotype (Q66824382)	chromosome abnormality (Q744962)	25395960
D009473	neuroplasticity (Q849491)	synaptic plasticity (Q1551556)	25396449
D040342	gene structure (Q30587678)	genetic structure (Q5532925)	25396043
D008461	meat product (Q1427887)	processed meat (Q23044244)	25395251
D004542	ejaculation (Q14820885)	Postorgasmic illness syndrome (Q2626291)	25396324
D059390	breakthrough pain (Q10503880)	pain (Q81938)	25394775
D060467	disease resistance (Q60790177)	plant disease resistance (Q4215946)	25395655
D016867	immunocompromised host (Q64732748)	immune disorder (Q3843811)	25395633
D004198	disease susceptibility (Q65534164)	susceptible individual (Q2624927)	25396551
D055170	nodulation (Q22298769)	root nodule (Q15098397)	25395023
D009043	motor activity (Q66970328)	cytoskeletal motor activity (Q14876109)	25395902
D052818	autotrophy (Q84953550)	autotroph (Q131427)	25395364
D004856	postural balance (Q98069141)	balance disorder (Q3540864)	25396523

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

Item in Mix'n'Match	Mix'n'match entry	External ID
sleep (Q35831)	25394707	D012894
	25394881	D012890
atmospheric pressure (Q81809)	25394691	D001274
	25395533	D000399
pain (Q81938)	25394775	D059390
	25395487	D010146
cell cycle (Q188941)	25394795	D002453
	25394838	D040681
chromosome abnormality (Q744962)	25395960	D059786
	25396268	D002869
gene duplication (Q746284)	25396508	D020440
	25395859	D020131
molecular geometry (Q911331)	25394883	D008968
	25396099	D015394
unplanned pregnancy (Q3817591)	25396549	D049168
	25395155	D011275
chromosomal fragile site (Q5113903)	25396441	D002873
	25395350	D043283
host-pathogen interaction (Q5909198)	25394535	D006790
	25394998	D054884
prenatal nutrition (Q7240527)	25394778	D020567
	25395033	D039401

Multiple items for the same external ID in Wikidata

External ID	Items in Mix'n'Match
D009055	mouth (Q9635) human mouth (Q1370895)
D064028	Tracheophyta (Q27133) conifer (Q132825)
D006967	allergy (Q42982) pet dander allergy (Q5481761) hypersensitivity (Q5958765)
D014754	violence (Q124490) violence prevention (Q104733130)
D011618	psychosis (Q170082) schizoaffective disorder (Q834047) schizophreniform disorder (Q2157462)
C023665	(−)-cathinone (Q414242) cathinone (Q7632116)
D010002	osteitis fibrosa cystica (Q799615) brown tumor (Q4976425)
D011693	purpura (Q935293) petechia (Q1412657)
C536209	congenital central hypoventilation syndrome (Q979129) Haddad syndrome (Q56014441)
C536281	pulmonary hemosiderosis (Q1052626) Alveolar hypoventilation syndrome (Q64425127)
D002613	cheilitis (Q1068997) cheilitis exfoliativa (Q1343695)
D000359	aftercare (Q4690707) aftercare (Q110537421)
C563020	anal canal carcinoma (Q2652259) cloacogenic carcinoma (Q18557499)
D017129	anisakiasis (Q3091959) anisakidosis (Q48782762)
D008199	adenitis (Q355981) lymphadenitis (Q3269466)
D007889	uterine fibroid (Q556281) leiomyoma (Q4667534)
C537436	Aromatase deficiency (Q4795506) aromatase excess syndrome (Q4795508)
D015451	chronic lymphocytic leukemia (Q1088156) small lymphocytic lymphoma (Q9022766)
C538208	Familial British dementia (Q5432926) ABri amyloidosis (Q50349602)
C535289	ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (Q940210) Rapp-Hodgkin syndrome (Q7294342)
C538090	surface epithelial-stromal tumor (Q7645976) ovarian carcinoma (Q18556145)
C535380	X-linked spinal muscular atrophy type 2 (Q8041562) infantile-onset X-linked spinal muscular atrophy (Q55345741)
C535523	infantile onset spinocerebellar ataxia (Q18553306) mitochondrial DNA depletion syndrome 7 (Q26492819)
C537743	Oguchi disease-1 (Q7080278) congenital stationary night blindness (Q18553290) hereditary night blindness (Q18557952)
C537206	spinocerebellar ataxia type 29 (Q21097773) spinocerebellar ataxia type 30 (Q21097774)
D064193	Anaphase promoting complex subunit 5 (Q21130504) anaphase-promoting complex subunit 5 (Q54438951)
D006841	aromatic compound (Q19834818) Hydrocarbons, Aromatic (Q21761549)
D001943	breast cancer (Q128581) breast neoplasm (Q23929670)
D008268	age related macular degeneration (Q830308) macular degeneration (Q27429789)
D014347	Trypanosoma brucei gambiense (Q9396337) Trypanosoma brucei gambiense (Q30216048)
C536868	hereditary spastic paraplegia 9A (Q32143434) autosomal dominant spastic paraplegia type 9 (Q55345928)
D006111	toxic diffuse goiter (Q16483) Graves' disease (Q50357588)
C535351	cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome (Q55345761) autosomal dominant optic atrophy plus syndrome (Q55345901)
C580039	mitochondrial DNA depletion syndrome 3 (Q26492815) mitochondrial DNA depletion syndrome, hepatocerebral form (Q55786491)
C538125	alopecia macular degeneration growth retardation syndrome (Q56014555) Kuster Majewski Hammerstein syndrome (Q56014598)
C564525	GATA 1 related cytopenia (Q3009546) thrombocytopenia with congenital dyserythropoietic anemia (Q56014250)
D004938	esophageal cancer (Q372701) esophageal neoplasm (Q56014520)
D026724	ethical review (Q56515249) medical ethical review (Q59094171)
D003331	coronary vessel (Q67315798) myocardial blood supply (Q106120773)
D004242	diving (Q7735) underwater diving (Q179643)
D007251	influenza (Q2840) swine influenza (Q36855)
D008168	lung (Q7886) human lung (Q2640512)
D009765	obesity (Q12174) epidemiology of obesity (Q5382727)
D006257	head (Q23640) human head (Q3409626)
D014714	Vertebrata (Q25241) vertebrate (Q110551902)
D001714	bipolar I disorder (Q4915474) bipolar disorder (Q131755)
D008607	intellectual disability (Q183560) idiot (Q193607) imbecile (Q4200185)
D004401	dysarthria (Q225957) scanning speech (Q7430080)
D016360	Clostridium difficile (Q310543) Clostridioides difficile Lawson et al. 2016 (Q56290719)
D010031	otitis (Q480700) Infectious otitis in animals (Q6054536)
D013734	androgen insensitivity syndrome (Q512313) Estrogen insensitivity syndrome (Q5401847)
D011009	pneumoconiosis (Q651223) bagassosis (Q4841462)
D012131	respiratory failure (Q767485) acute respiratory insufficiency (Q21006662)
D003486	cyanide poisoning (Q883082) cyanide (Q55076544)
D005538	American football (Q41323) football codes (Q1081491)
D003607	dacryocystitis (Q1157761) dacryoadenitis (Q1424488)
D003711	demyelination (Q1186697) demyelinating disease (Q1186703)
C537492	Stickler syndrome (Q2288646) Stickler syndrome type 1 (Q55345651)
D000309	adrenal insufficiency (Q2507454) hypoadrenalism (Q10939641)
D013502	general surgery (Q932510) history of surgery (Q2556088)
D011502	marasmus (Q582904) protein-energy malnutrition (Q4082071)
D013274	stomach cancer (Q189588) stomach neoplasm (Q4335552)
D014438	typhus (Q160649) epidemic typhus (Q1290616)
C535504	autosomal recessive multiple epiphyseal dysplasia (Q3042144) autosomal recessive multiple epiphyseal dysplasia (Q60195170)
D000158	Tympanometry (Q1671504) impedance audiometry (Q3307114)
D014689	chronic cerebrospinal venous insufficiency (Q1088054) venous insufficiency (Q9008818)
D010854	black piedra (Q2059411) piedra (Q10863066)
C535952	eosinophilic gastritis (Q18556159) eosinophilic gastroenteritis (Q27555722)
C536377	nonsyndromic congenital nail disorder 4 (Q18553374) anonychia congenita (Q22443772)
C536943	tarsal-carpal coalition syndrome (Q18553474) calcaneonavicular coalition (Q18554815)
D046110	gestational hypertension (Q1519482) hypertensive disease of pregnancy (Q19001368)
D053450	TNF receptor superfamily member 18 (Q21135817) tumor necrosis factor receptor 18 (Q24784554)
D001619	beta-hexosaminidase (Q24745388) hexosaminidase D (Q54461946)
C016766	(+/-)-sulforaphane (Q424489) (R)-sulforaphane (Q27120804)
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)
C536664	Zellweger spectrum disorder (Q51250082) peroxisomal biogenesis disorder (Q61913385)
D004932	esophageal varix (Q298278) esophageal and gastric varices (Q54911777)
C538388	X-linked hypertrichosis (Q8041556) X-linked congenital generalized hypertrichosis (Q55345748)
D002113	calcification (Q933382) calcification (Q71159138)
C565637	deafness, sensorineural, autosomal-mitochondrial type (Q55781811) autosomal-mitochondrial sensorineural deafness (Q102293457)
D006321	heart (Q1072) human heart (Q2419844)
D013991	Tietze syndrome (Q175763) costochondritis (Q5175170)
D004541	Eisenmenger's syndrome (Q572695) Eisenmenger complex (Q1313103)
D053716	Relative energy deficiency in sport (Q755630) female athlete triad syndrome (Q109310870)
D014314	trisomy (Q844903) Warkany syndrome (Q2454191)
D011695	Henoch-Schoenlein purpura (Q1035319) Henoch-Schönlein nephritis (Q16611043)
D066194	rhinencephalon (Q1153195) olfactory cortex (Q70750040)
D001859	bone neoplasm (Q1328805) bone sarcoma (Q56014469)
D002313	restrictive cardiomyopathy (Q2151267) acute pericarditis (Q3232575)
D051379	Mus (Q39275) mouse (Q2751034)
D018270	invasive ductal carcinoma (Q1671685) breast ductal carcinoma (Q3658404)
D009477	congenital insensitivity to pain with anhidrosis (Q501694) hereditary sensory and autonomic neuropathy (Q3702898)
C535576	Heart valve dysplasia (Q5692507) X-linked cardiac valvular dysplasia (Q102293803)
C536085	Ichthyosis follicularis with alopecia and photophobia syndrome (Q5986440) ichthyosis follicularis-alopecia-photophobia syndrome 1 (Q102293700)
D008548	freckle (Q187882) melanosis (Q6811539)
D010051	ovarian cancer (Q172341) ovarian neoplasm (Q11793790)
C535358	choroidal sclerosis (Q18558226) central areolar choroidal dystrophy (Q55345702)
D018332	Spitz nevus (Q2311457) epithelioid and spindle cell nevus (Q18971640)
C535444	alpha-methylacyl-CoA racemase deficiency (Q27164415) congenital bile acid synthesis defect 4 (Q42863600)
D012893	sleep disorder (Q177190) sleep-wake disorder (Q54972453)
C580174	Huntington's disease-like syndrome (Q24977062) Huntington disease and related disorders (Q55345637)
C565089	calvarial doughnut lesions-bone fragility syndrome (Q55780509) calvarial doughnut lesions-bone fragility syndrome (Q102293214)
D002583	cervix uterine cancer (Q160105) uterine cervix neoplasm (Q56014502)
D012867	skin (Q1074) human skin (Q5259911)
D008103	liver cirrhosis (Q147778) cirrosis (Q12569389)
C027576	4-hydroxy-2-nonenal (Q229982) 4-hydroxynonenal (Q74428599)
D005820	genetic testing (Q285223) genetic screen (Q5050812)
D001924	concussion (Q326921) concussion (Q16302928)
D000361	agammaglobulinemia (Q1047559) agammaglobulinemia (Q5659619)
D054380	C-X-C motif chemokine receptor 5 (Q1024612) CXC chemokine receptor 5 (Q24727201)
D010000	bone inflammation disease (Q1178507) Osteítis (Q21141385)
D000168	Pfeiffer syndrome (Q1286848) acrocephalosyndactylia (Q1786496) Saethre-Chotzen syndrome (Q3508686)
D012772	toxic shock syndrome (Q1128440) septic shock (Q1765564)
D011906	sodoku (Q1807401) rat-bite fever (Q2754970)
D010009	multiple epiphyseal dysplasia (Q1452604) osteochondrodysplasia (Q3251367)
D050644	Succinate-semialdehyde dehydrogenase (NAD+) (Q3976579) Succinate-semialdehyde dehydrogenase (NAD(P)+) (Q3976581)
C538187	Acrogeria (Q4675775) metageria (Q6822520)
D010190	pancreatic cancer (Q212961) pancreatic neoplasm (Q7130412)
C562924	Dowling-Degos disease (Q7316720) reticulate acropigmentation of Kitamura (Q7316721)
C536252	metaphyseal dysplasia (Q13566985) Metaphyseal dysplasia, Pyle type (Q22965556)
D014897	spinal muscular atrophy (Q580290) juvenile spinal muscular atrophy (Q18554312)
C580473	mitochondrial DNA depletion syndrome 5 (Q26492817) mitochondrial DNA depletion syndrome 9 (Q26492821)
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)
C537240	progressive supranuclear palsy-parkinsonism syndrome (Q55345717) atypical progressive supranuclear palsy syndrome (Q55346109)
C536214	cold-induced sweating syndrome (Q3961672) Crisponi syndrome (Q55998740)
C563162	familial calcium pyrophosphate deposition (Q55950198) calcium pyrophosphate dihydrate crystal deposition disease (Q64348505)
C538618	paroxysmal cold hemoglobinuria (Q734042) Donath–Landsteiner hemolytic anemia (Q65120981)
D000971	chemotherapy regimen (Q5090632) antineoplastic combined chemotherapy protocols (Q66764603)
C565535	granulocytopenia with immunoglobulin abnormality (Q55781920) immunodeficiency 59 (Q102294307)
D000086382	COVID-19 (Q84263196) COVID-19 mortality (Q104778232)
D012886	human skull (Q9604) skull (Q13147)
D010554	personality disorder (Q270673) avoidant personality disorder (Q509122) narcissistic personality disorder (Q1060310)
D058531	XX male syndrome (Q365589) XX male syndrome (Q28401082)
D001921	brain (Q1073) human brain (Q492038)
C537724	Lujan–Fryns syndrome (Q640836) syndromic X-linked intellectual disability 14 (Q28065625)
D009369	cancer (Q12078) neoplasm (Q1216998)
D010259	delusional disorder (Q721073) paranoia (Q1229994)
D000037	placental abruption (Q388113) acute pancreatitis (Q854573)
D002543	cerebral hemorrhage (Q1368943) hereditary cystatin C amyloid angiopathy (Q10992004)
D056587	Muckle-Wells syndrome (Q1538218) cryopyrin-associated periodic syndrome (Q1771331) familial cold urticaria (Q1835481)
D000224	Addison's disease (Q8282) hyperthermia (Q242165)
D016472	lateral sclerosis (Q2881413) motor neuron disease (Q3221083)
D009221	fibrodysplasia ossificans progressiva (Q1410831) myositis ossificans (Q3858675)
D008334	mandible (Q16370) human mandible (Q5283631)
D010412	penile cancer (Q1342955) penile neoplasm (Q18554121)
D020921	sleep sex (Q1637663) sleep arousal disorder (Q19001302)
C041376	rosmarinic acid (Q7762) (R)-rosmarinic acid (Q50380051)
D050090	true hermaphroditism (Q7847568) ovotesticular disorder of sex development (Q54944059)
C536350	mitochondrial DNA depletion syndrome 1 (Q6881876) mitochondrial DNA depletion syndrome 8a (Q26492820) oculogastrointestinal muscular dystrophy (Q55782392) mitochondrial DNA depletion syndrome 8b (Q63859996)
D013736	testicular cancer (Q324464) tumor of testis and paratestis (Q55787784)
C535761	familial nephrotic syndrome (Q2160802) nephrotic syndrome type 1 (Q61913400)
C536522	X-linked myopathy with excessive autophagy (Q3456637) Autophagic vacuolar myopathy (Q63874868)
D006394	hemangiosarcoma (Q539728) angiosarcoma (Q2619091)
D002375	waxy flexibility (Q460263) catalepsy (Q918193)
D007174	kleptomania (Q212021) impulse control disorder (Q1201835)
D016735	factitious disorder imposed on another (Q1414765) factitious disorder imposed on another (Q48783155)
D002663	babbling (Q1723890) children's language (Q1741898)
D018249	oxyphilic adenoma (Q1760202) Hurthle cell (Q4223446)
D003924	maturity-onset diabetes of the young (Q663041) type 2 diabetes (Q3025883)
D019556	COS cell line (Q5013524) COS-7 (Q27556092)
C566897	Ligneous conjunctivitis (Q6546687) plasminogen deficiency type I (Q97109018)
C535564	hypoplastic tibiae-postaxial polydactyly syndrome (Q17122962) absent tibia-polydactyly syndrome (Q56014402)
D044464	F2R like trypsin receptor 1 (Q21115613) protease-activated receptor 2 (Q24722679)
D014594	uterine cancer (Q1209744) uterine neoplasm (Q56014517)
D009666	nose (Q7363) human nose (Q2673594)
D001022	aortic valve insufficiency (Q616087) Duroziez's sign (Q3773831)
D004326	drinking (Q876776) water consumption (Q1277412)
D008209	lymphedema (Q916398) hereditary lymphedema (Q1996246)
D006223	Cowden syndrome 1 (Q1138188) Lhermitte–Duclos disease (Q1461101) multiple hamartoma syndrome (Q3508737)
D012734	pseudohermaphroditism (Q2273662) disorder of sex development (Q5282521)
D001327	type II hypersensitivity (Q5898312) autoimmune disease (Q8084905)
D007822	laryngeal cancer (Q852423) laryngeal neoplasm (Q18555128)
D007876	Pontiac fever (Q3073142) legionellosis (Q18553869)
D005715	gambling (Q11416) problem gambling (Q748309)
D011014	pneumonia (Q12192) pneumonitis (Q1284347)
D002145	corn (Q154558) callosity (Q579108)
D016464	lysosomal storage disease (Q675010) Q16562088
D005525	food manufacturer (Q1252971) food manufacturing (Q2836940)
D014211	bejel (Q682798) treponematosis (Q1243869)
D004480	ectromelia (Q1323724) fibular hemimelia (Q1411024)
D010373	Pediculus humanus capitis infestation (Q532158) lice infestation (Q1343674)
D016906	Interleukin 9 (Q2563463) Interleukin-9 (Q24787897)
D010282	parathyroid carcinoma (Q40301) parathyroid neoplasm (Q7136148)
D029461	Salla disease (Q3843807) sialuria (Q7506696)
D000857	parosmia (Q1759234) olfaction disorder (Q11419348)
C536535	venous aneurysm (Q5676399) Vein of Galen aneurysmal malformations (Q11766796)
D013964	thyroid cancer (Q826522) thyroid neoplasm (Q13632630)
D012170	central retinal vein occlusion (Q190831) retinal vein occlusion (Q18554884)
D001749	bladder cancer (Q504775) bladder neoplasm (Q55949884)
D006001	glycoconjugate (Q416019) glycoconjugates [Golgi lumen] (Q50268135)
C563835	drug metabolism, poor, Cyp2D6-related (Q55783616) Poor drug metabolism (Q109905255)
D010731	phosphoenolpyruvate-dependent sugar phosphotransferase system (Q21199241) PTS-GFL superfamily (Q25112332) PTS-AG superfamily (Q28209150)
D057809	HEK293 (Q489618) HEK293T (Q27546876)
C566917	Glycogen storage disease type 0 (Q5572606) glycogen storage disease type 0B (Q109676512)