User:Magnus Manske/Mix'n'match report/663

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 Diseases

Medical Subject Headings for Diseases

Unknown external ID

• 33472 external IDs in Wikidata but not in Mix'n'Match. Too many to show individually.

Different items for the same external ID

• 616 enties have different items on Mix'n'match and Wikidata. Too many to show individually.

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

Item in Mix'n'Match	Mix'n'match entry	External ID	External label
headache (Q86)	25731714	D006261	Headache
	25732384	D020773	Headache Disorders
hepatitis B (Q6853)	25732126	D006509	Hepatitis B
	25731192	D019694	Hepatitis B, Chronic
deafness (Q12133)	25734168	D003638	Deafness
	25732396	D006315	Hearing Loss, Functional
	25735102	D034381	Hearing Loss
	25732834	D046089	Hearing Loss, Mixed Conductive-Sensorineural
frontotemporal lobar degeneration (Q18579)	25731991	D003704	Dementia
	25732618	D057174	Frontotemporal Lobar Degeneration
miscarriage (Q28693)	25733143	D000022	Abortion, Spontaneous
	25731137	D020964	Embryo Loss
carcinoma (Q33525)	25731858	D002277	Carcinoma
	25732689	D009375	Neoplasms, Glandular and Epithelial
syphilis (Q41083)	25730743	D002601	Chancre
	25730772	D013587	Syphilis
enthesopathy (Q52844)	25732371	D000070676	Enthesopathy
	25730819	D012216	Rheumatic Diseases
Lemierre's syndrome (Q72000)	25735243	D005674	Fusobacterium Infections
	25735020	D057831	Lemierre Syndrome
pain (Q81938)	25734297	D010146	Pain
	25732179	D059390	Breakthrough Pain
hepatitis (Q131742)	25731726	D006505	Hepatitis
	25735052	D006521	Hepatitis, Chronic
diphtheria (Q134649)	25733169	D003354	Corynebacterium Infections
	25730799	D004165	Diphtheria
pertussis (Q134859)	25731562	D001885	Bordetella Infections
	25732766	D014917	Whooping Cough
hepatitis C (Q154869)	25733982	D006526	Hepatitis C
	25731526	D019698	Hepatitis C, Chronic
leptospirosis (Q155098)	25735196	D007922	Leptospirosis
	25732751	D014895	Weil Disease
osteoporosis (Q165328)	25734085	D010024	Osteoporosis
	25732389	D015663	Osteoporosis, Postmenopausal
kidney stone disease (Q178623)	25732702	D000069856	Staghorn Calculi
	25735009	D007669	Kidney Calculi
sickle-cell disease (Q185034)	25732058	D000755	Anemia, Sickle Cell
	25732192	D006450	Hemoglobin SC Disease
Zenker's diverticulum (Q189638)	25730564	D004936	Diverticulum, Esophageal
	25731374	D016672	Zenker Diverticulum
cerebral amyloid angiopathy (Q191562)	25734474	D016657	Cerebral Amyloid Angiopathy
	25731601	D028243	Cerebral Amyloid Angiopathy, Familial
ataxia (Q213373)	25733837	D001259	Ataxia
	25733782	D020234	Gait Ataxia
bronchospasm (Q279330)	25732258	D001982	Bronchial Diseases
	25733732	D001986	Bronchial Spasm
cholecystitis (Q376666)	25734305	D002764	Cholecystitis
	25734546	D041881	Cholecystitis, Acute
post-thrombotic syndrome (Q382091)	25733415	D011186	Postphlebitic Syndrome
	25733862	D054070	Postthrombotic Syndrome
placental abruption (Q388113)	25733668	D000033	Abortion, Threatened
	25732013	D000037	Abruptio Placentae
bilirubin metabolic disorder (Q390475)	25732127	D006932	Hyperbilirubinemia
	25733321	D006933	Hyperbilirubinemia, Hereditary
bronchiolitis (Q424227)	25732135	D001988	Bronchiolitis
	25731481	D001990	Bronchiolitis, Viral
Takayasu's arteritis (Q432462)	25731485	D001015	Aortic Arch Syndromes
	25732082	D013625	Takayasu Arteritis
lower urinary tract symptoms (Q446372)	25734448	D053448	Prostatism
	25734786	D059411	Lower Urinary Tract Symptoms
anal fissure (Q484797)	25732713	D001004	Anus Diseases
	25734091	D005401	Fissure in Ano
osteosarcoma (Q549534)	25731551	D012516	Osteosarcoma
	25733878	D018213	Neoplasms, Bone Tissue
vascular dementia (Q583908)	25731296	D015140	Dementia, Vascular
	25730993	D015161	Dementia, Multi-Infarct
photodermatitis (Q608085)	25731304	D010787	Photosensitivity Disorders
	25731506	D017454	Dermatitis, Photoallergic
renal colic (Q609202)	25731377	D014514	Ureteral Calculi
	25732865	D056844	Renal Colic
dislocation of hip (Q634638)	25731539	D006617	Hip Dislocation
	25735260	D006618	Hip Dislocation, Congenital
rickettsiosis (Q646664)	25733873	D012282	Rickettsia Infections
	25732899	D012288	Rickettsiaceae Infections
long QT syndrome (Q653924)	25733309	D008133	Long QT Syndrome
	25734872	D029597	Romano-Ward Syndrome
squamous cell carcinoma (Q681817)	25732223	D002294	Carcinoma, Squamous Cell
	25732220	D018307	Neoplasms, Squamous Cell
arteriovenous fistula (Q707837)	25731793	D001164	Arteriovenous Fistula
	25733847	D016157	Vascular Fistula
bacterial infectious disease (Q727028)	25730550	D001424	Bacterial Infections
	25733868	D016905	Gram-Negative Bacterial Infections
	25735236	D016908	Gram-Positive Bacterial Infections
chronic renal insufficiency (Q736715)	25731785	D007676	Kidney Failure, Chronic
	25730681	D051436	Renal Insufficiency, Chronic
pulmonary aspiration (Q737510)	25731782	D053120	Respiratory Aspiration
	25732064	D063466	Respiratory Aspiration of Gastric Contents
subclavian steal syndrome (Q742099)	25734117	D013349	Subclavian Steal Syndrome
	25732983	D058686	Coronary-Subclavian Steal Syndrome
chromosome abnormality (Q744962)	25731635	D002869	Chromosome Aberrations
	25732132	D059786	Abnormal Karyotype
respiratory failure (Q767485)	25733075	D012131	Respiratory Insufficiency
	25735142	D012133	Respiratory Paralysis
basal-cell carcinoma (Q809758)	25734567	D002280	Carcinoma, Basal Cell
	25734657	D018295	Neoplasms, Basal Cell
dysphonia (Q836379)	25730678	D006685	Hoarseness
	25732927	D055154	Dysphonia
adenovirus infection (Q837054)	25730926	D000257	Adenoviridae Infections
	25730835	D000258	Adenovirus Infections, Human
coronary artery disease (Q844935)	25733209	D003324	Coronary Artery Disease
	25731561	D003327	Coronary Disease
	25731557	D017202	Myocardial Ischemia
neurofibromatoses (Q847605)	25732826	D009456	Neurofibromatosis 1
	25732608	D016518	Neurofibromatosis 2
	25733801	D017253	Neurofibromatoses
lymphadenopathy (Q847726)	25734914	D000072281	Lymphadenopathy
	25730787	D008206	Lymphatic Diseases
hallux valgus (Q852574)	25735084	D000071378	Bunion
	25734751	D006215	Hallux Valgus
dystonia (Q906492)	25731027	D004421	Dystonia
	25730528	D020821	Dystonic Disorders
sensorineural hearing loss (Q928697)	25731039	D006313	Hearing Loss, Central
	25734852	D006316	Hearing Loss, High-Frequency
	25731820	D006319	Hearing Loss, Sensorineural
skin disease (Q949302)	25734049	D012871	Skin Diseases
	25733563	D012873	Skin Diseases, Genetic
amebiasis (Q949694)	25734303	D000562	Amebiasis
	25732217	D004749	Entamoebiasis
myelodysplastic syndrome (Q954625)	25734624	D009190	Myelodysplastic Syndromes
	25732839	D011289	Preleukemia
XY gonadal dysgenesis (Q957751)	25733287	D006061	Gonadal Dysgenesis, 46,XY
	25734425	D058490	46, XY Disorders of Sex Development
liver failure (Q970208)	25730693	D017093	Liver Failure
	25732481	D048550	Hepatic Insufficiency
eczema (Q988594)	25733748	D004485	Eczema
	25734068	D017443	Skin Diseases, Eczematous
bruxism (Q994942)	25734797	D002012	Bruxism
	25732997	D020186	Sleep Bruxism
gingival and periodontal pocket (Q1059860)	25734987	D005888	Gingival Pocket
	25731285	D010514	Periodontal Pocket
temporomandibular joint syndrome (Q1068323)	25734221	D013705	Temporomandibular Joint Disorders
	25732111	D013706	Temporomandibular Joint Dysfunction Syndrome
hypohidrotic ectodermal dysplasia (Q1077955)	25734773	D053358	Ectodermal Dysplasia 1, Anhidrotic
	25731373	D053359	Ectodermal Dysplasia 3, Anhidrotic
mandibular fracture (Q1127367)	25735066	D007572	Jaw Fractures
	25733093	D008337	Mandibular Fractures
Ewing sarcoma (Q1138580)	25731284	D012512	Sarcoma, Ewing
	25732219	D018241	Neuroectodermal Tumors, Primitive, Peripheral
heat illness (Q1191065)	25731313	D018882	Heat Stress Disorders
	25734013	D018883	Heat Stroke
herpes simplex virus keratitis (Q1258984)	25734256	D007635	Keratitis, Dendritic
	25734866	D016849	Keratitis, Herpetic
vascular disease (Q1266890)	25734750	D014652	Vascular Diseases
	25730963	D020758	Spinal Cord Vascular Diseases
	25730643	D020760	Spinal Cord Ischemia
oroantral fistula (Q1277281)	25731309	D003751	Dental Fistula
	25732232	D009957	Oroantral Fistula
fibrosarcoma (Q1362453)	25733909	D005354	Fibrosarcoma
	25731711	D018218	Neoplasms, Fibrous Tissue
hypertrophic cardiomyopathy (Q1364270)	25731318	D002312	Cardiomyopathy, Hypertrophic
	25732316	D024741	Cardiomyopathy, Hypertrophic, Familial
cerebral hemorrhage (Q1368943)	25732085	D020201	Brain Hemorrhage, Traumatic
	25732821	D020202	Cerebral Hemorrhage, Traumatic
spinal cord injury (Q1415275)	25732819	D013119	Spinal Cord Injuries
	25730962	D013124	Spinal Injuries
foreign body granuloma (Q1455131)	25734328	D005549	Foreign-Body Reaction
	25731508	D015745	Granuloma, Foreign-Body
lipid metabolism disorder (Q1476525)	25732174	D050171	Dyslipidemias
	25734089	D052439	Lipid Metabolism Disorders
failure to thrive (Q1497481)	25731874	D005183	Failure to Thrive
	25732152	D006130	Growth Disorders
venous ulcer (Q1573613)	25734694	D007871	Leg Ulcer
	25732176	D014647	Varicose Ulcer
urolithiasis (Q1585769)	25732412	D014545	Urinary Calculi
	25733984	D052878	Urolithiasis
sialolithiasis (Q1627831)	25734652	D012465	Salivary Duct Calculi
	25734683	D015494	Salivary Gland Calculi
	25734923	D020792	Salivary Calculi
neonatal jaundice (Q1755487)	25733614	D007567	Jaundice, Neonatal
	25731427	D051556	Hyperbilirubinemia, Neonatal
myeloproliferative disorders (Q1898104)	25731085	D009196	Myeloproliferative Disorders
	25734443	D019046	Bone Marrow Neoplasms
viral hepatitis (Q1983841)	25733809	D006524	Hepatitis, Viral, Animal
	25733291	D006525	Hepatitis, Viral, Human
enterobiasis (Q1992236)	25731087	D010123	Oxyuriasis
	25733660	D017229	Enterobiasis
pharyngitis (Q2085267)	25734097	D010608	Pharyngeal Diseases
	25731978	D010612	Pharyngitis
congenital diaphragmatic hernia (Q2163245)	25734152	D006548	Hernia, Diaphragmatic
	25735220	D065630	Hernias, Diaphragmatic, Congenital
gastrointestinal system disease (Q2300099)	25732867	D004066	Digestive System Diseases
	25733476	D005767	Gastrointestinal Diseases
synovial chondromatosis (Q2376149)	25735049	D015838	Chondromatosis, Synovial
	25735206	D018210	Chondromatosis
gingival overgrowth (Q2637111)	25733826	D005885	Gingival Hyperplasia
	25732166	D019214	Gingival Overgrowth
small-intestine disease (Q2852245)	25734047	D004378	Duodenal Diseases
	25731467	D007579	Jejunal Diseases
diastasis (Q3026419)	25733638	D000070630	Diastasis, Muscle
	25733421	D000070631	Diastasis, Bone
subdural hematoma (Q3144926)	25731534	D006408	Hematoma, Subdural
	25730627	D020199	Hematoma, Subdural, Acute
	25730622	D020200	Hematoma, Subdural, Chronic
	25731815	D046648	Hematoma, Subdural, Intracranial
	25730954	D046649	Hematoma, Subdural, Spinal
Niemann–Pick disease, SMPD1-associated (Q3281285)	25732251	D009542	Niemann-Pick Diseases
	25731695	D052536	Niemann-Pick Disease, Type A
respiratory disease (Q3286546)	25731571	D012120	Respiration Disorders
	25734167	D012140	Respiratory Tract Diseases
colonic neoplasm (Q3542029)	25730536	D003110	Colonic Neoplasms
	25733185	D015179	Colorectal Neoplasms
environmental disease (Q3751709)	25732816	D007280	Disorders of Environmental Origin
	25730585	D018876	Environmental Illness
scrofula (Q4678337)	25735154	D014388	Tuberculosis, Lymph Node
	25730956	D018601	King's Evil
carcinosarcoma (Q5038170)	25730729	D002296	Carcinosarcoma
	25734135	D018199	Mixed Tumor, Mesodermal
	25732649	D018200	Mixed Tumor, Mullerian
clear cell adenocarcinoma (Q5130800)	25732804	D008649	Mesonephroma
	25731224	D018262	Adenocarcinoma, Clear Cell
enchondromatosis (Q5375429)	25733813	D004687	Enchondromatosis
	25734675	D010009	Osteochondrodysplasias
gastrointestinal system cancer (Q5526839)	25734985	D004067	Digestive System Neoplasms
	25733090	D005770	Gastrointestinal Neoplasms
humerus fracture (Q5940721)	25734714	D006810	Humeral Fractures
	25734401	D012784	Shoulder Fractures
intraventricular hemorrhage (Q6058597)	25734499	D002543	Cerebral Hemorrhage
	25734169	D002832	Choroid Hemorrhage
gout attack (Q6081223)	25730891	D006073	Gout
	25731253	D015210	Arthritis, Gouty
placenta disease (Q7200296)	25731659	D010922	Placenta Diseases
	25735265	D011248	Pregnancy Complications
primary hyperoxaluria (Q7243137)	25731696	D006959	Hyperoxaluria
	25730644	D006960	Hyperoxaluria, Primary
nervous system cancer (Q16918477)	25733569	D009380	Neoplasms, Nerve Tissue
	25733319	D009423	Nervous System Neoplasms
intestinal schistosomiasis (Q18553329)	25732942	D012554	Schistosomiasis japonica
	25730669	D012555	Schistosomiasis mansoni
familial hyperlipidemia (Q18554145)	25731839	D006949	Hyperlipidemias
	25732259	D006951	Hyperlipoproteinemias
22q11 deletion syndrome (Q18554351)	25733675	D004062	DiGeorge Syndrome
	25734312	D058165	22q11 Deletion Syndrome
central nervous system tuberculosis (Q18554860)	25732734	D016862	Tuberculoma, Intracranial
	25733389	D020306	Tuberculosis, Central Nervous System
gangliocytoma (Q18555074)	25734260	D005729	Ganglioneuroma
	25731544	D018303	Ganglioglioma
Spinal cord cancer (Q18556900)	25733653	D013120	Spinal Cord Neoplasms
	25730709	D013125	Spinal Neoplasms
muscle neoplasm (Q18975957)	25731602	D009379	Neoplasms, Muscle Tissue
	25732743	D019042	Muscle Neoplasms
peripheral vascular disease (Q26695607)	25735261	D001157	Arterial Occlusive Diseases
	25733208	D016481	Helicobacter Infections
	25733620	D016491	Peripheral Vascular Diseases
Surgical shock (Q30315175)	25731725	D012773	Shock, Surgical
	25731089	D016063	Blood Loss, Surgical
jaw disease (Q47108021)	25735032	D007571	Jaw Diseases
	25734149	D008336	Mandibular Diseases

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)
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)
D000037	placental abruption (Q388113) acute pancreatitis (Q854573)
D000086382	COVID-19 (Q84263196) COVID-19 mortality (Q104778232)
D000158	tympanometry (Q1671504) impedance audiometry (Q3307114)
D000168	Pfeiffer syndrome (Q1286848) acrocephalosyndactylia (Q1786496) Saethre-Chotzen syndrome (Q3508686)
D000224	Addison's disease (Q8282) hyperthermia (Q242165)
D000309	adrenal insufficiency (Q2507454) hypoadrenalism (Q10939641)
D000359	aftercare (Q4690707) aftercare (Q110537421)
D000361	agammaglobulinemia (Q1047559) agammaglobulinemia (Q5659619)
D000857	parosmia (Q1759234) olfaction disorder (Q11419348)
D000971	chemotherapy regimen (Q5090632) antineoplastic combined chemotherapy protocols (Q66764603)
D001022	aortic valve insufficiency (Q616087) Duroziez's sign (Q3773831)
D001327	type II hypersensitivity (Q5898312) autoimmune disease (Q8084905)
D001619	beta-hexosaminidase (Q24745388) hexosaminidase D (Q54461946)
D001714	bipolar disorder (Q131755) bipolar I disorder (Q4915474)
D001749	bladder cancer (Q504775) bladder neoplasm (Q55949884)
D001859	bone neoplasm (Q1328805) bone sarcoma (Q56014469)
D001921	brain (Q1073) human brain (Q492038)
D001924	concussion (Q326921) concussion (Q16302928)
D001943	breast cancer (Q128581) breast neoplasm (Q23929670)
D002113	calcification (Q933382) calcification (Q71159138)
D002145	corn (Q154558) callosity (Q579108)
D002313	restrictive cardiomyopathy (Q2151267) acute pericarditis (Q3232575)
D002375	waxy flexibility (Q460263) catalepsy (Q918193)
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)
D002663	babbling (Q1723890) children's language (Q1741898)
D003331	coronary vessel (Q67315798) myocardial blood supply (Q106120773)
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)
D004932	esophageal varix (Q298278) esophageal and gastric varices (Q54911777)
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)
D007251	influenza (Q2840) swine influenza (Q36855)
D007822	laryngeal cancer (Q852423) laryngeal neoplasm (Q18555128)
D007876	Pontiac fever (Q3073142) legionellosis (Q18553869)
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) idiot (Q193607) 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)
D011693	purpura (Q935293) petechia (Q1412657)
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) Sindrome de anuel AA (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)
D016360	Clostridium difficile (Q310543) Clostridioides difficile Lawson et al. 2016 (Q56290719)
D016464	lysosomal storage disease (Q675010) Q16562088
D016472	lateral sclerosis (Q2881413) motor neuron disease (Q3221083)
D016735	factitious disorder imposed on another (Q1414765) factitious disorder imposed on another (Q48783155)
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)
D053716	relative energy deficiency in sport (Q755630) female athlete triad syndrome (Q109310870)
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	Tracheophytes (Q27133) conifer (Q132825)
D064193	Anaphase promoting complex subunit 5 (Q21130504) anaphase-promoting complex subunit 5 (Q54438951)
D066194	rhinencephalon (Q1153195) olfactory cortex (Q70750040)