Wikidata:WikiProject Source MetaData/Wikidata lists/Usage of Scholia in Template Medical resources on the English Wikipedia

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This page lists items for which the English-language Wikipedia article links to Scholia profiles via Template:Medical resources, which complements links via Template:Scholia, which are tracked separately.


This list is periodically updated by a bot. Manual changes to the list will be removed on the next update!

WDQS | PetScan | TABernacle | Find images Recent changes | Query: SELECT DISTINCT ?item WHERE { { SELECT ?item WHERE { SERVICE wikibase:mwapi { bd:serviceParam wikibase:endpoint "" . bd:serviceParam wikibase:api "Generator" . bd:serviceParam mwapi:generator "search" . bd:serviceParam mwapi:gsrsearch "scholia hastemplate:\"Medical resources\"" . bd:serviceParam mwapi:gsrlimit "max" . ?item wikibase:apiOutputItem mwapi:item . } } LIMIT 1000 } hint:Prior hint:runFirst "true". } LIMIT 1000


image Article description instance of
Blood culture negative endocarditis.jpg
endocarditis endocardium disease characterized by inflammation of the endocardium of the heart chambers and valves
ERCP cholangioca.jpg
cholangiocarcinoma bile duct adenocarcinoma that has material basis in bile duct epithelial cells.
coma state of unconsciousness
hyperopia visual defect which causes to see the far objects clearly and near objects unclearly
Cerebral amyloid angiopathy - very high mag.jpg
cerebral amyloid angiopathy amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes
cesarean section surgical procedure in which a baby is delivered through a mother's abdomen
anosmia the inability to smell
eclampsia pre-eclampsia characterized by the presence of seizures
cholangitis bile duct disease that is an inflammation of the bile duct
Myxomatous aortic valve.jpg
aortic valve insufficiency aortic valve disease that is characterized by leaking of the aortic valve of the heart causes blood to flow in the reverse direction during ventricular diastole, from the aorta into the left ventricle
Vestibulocerebellar syndrome medical condition
autoimmune polyendocrine syndrome autoimmune disease of endocrine system with auto-reactivity against endocrine organs
Bernard-Soulier syndrome Human disease
fat embolism type of embolism
congenital muscular dystrophy human disease
hepatomegaly symptom
autoimmune polyendocrine syndrome type 2 An autoimmune polyendocrine syndrome that is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs. It is more heterogeneous and has not been linked to one gene.
acute proliferative glomerulonephritis Human disease
hemophilia A X-linked disease that has material basis in Factor VIII deficiency, which results in the formation of fibrin deficient clots which makes coagulation much more prolonged
Haemophilus parainfluenzae Endocarditis PHIL 851 lores.jpg
infective endocarditis endocarditis that is characterized by inflammation of the endocardium caused by infectious agents.
hemophilia B An inherited blood coagulation disease that has material basis in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.
1471-2415-12-28-1Cerebral angiogram.jpg
cerebrovascular disease artery disease that is characterized by dysfunction of the blood vessels supplying the brain
constrictive pericarditis heart disorder in which the pericardial sac becomes thickened and fibrotic, tightening the myocardium and impeding the normal myocardial function
hemopericardium pericardial effusion that results from blood in the pericardial sac
autosomal recessive polycystic kidney recessive form of polycystic kidney disease
hyperpituitarism endocrine disease
Cytomegalovirus retinitis retinitis that has material basis in Cytomegalovirus
Skin Tumors-010.jpg
acral lentiginous melanoma kind of lentiginous skin melanoma
Buschke–Ollendorff syndrome medical condition
complement deficiency primary immunodeficiency disease that is the result in a mutation of a gene encoding one of the thirty complement system proteins, produced predominantly in liver, which function to defend against infection and produce inflammation
Deficiency of the interleukin-1–receptor antagonist An autoinflammatory disease caused by mutations in the IL1RN gene, which encodes the IL1 receptor antagonist. It presents in infancy, and is characterized by systemic inflammation, pustular rash, bone pain, sterile osteitis, and periostitis.
Humoral immune deficiency medical condition
ischemic cardiomyopathy type of cardiomyopathy caused by a narrowing of the coronary arteries which supply blood to the heart
Endo dysfunction Athero.PNG
atherosclerosis form of arteriosclerosis
glycogen storage disease IX glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity
Idiopathic sclerosing mesenteritis medical condition
Snellen chart.svg
Childhood blindness medical condition
Autosomal dominant - en.svg
Activated PI3K Delta Syndrome medical condition
Symptoms of leukemia.png
leukemia group of cancers that usually begin in the bone marrow
Blue circle for diabetes.svg
type-1 diabetes form of diabetes mellitus
Schistosomiasis itch.jpeg
schistosomiasis human disease
sputum mucus that is coughed up from the lower airways
protein-losing enteropathy Human disease
thrombophlebitis phlebitis that results from a blood clot in the vessel
Diffuse proliferative lupus nephritis.jpg
nephritis inflammation of the kidneys
radial neuropathy Human disease
Стеноз ниркової артерії.jpg
renal artery obstruction narrowing of one of the renal arteries, most often caused by atherosclerosis or fibromuscular dysplasia
pulmonary valve stenosis Human disease
pancreatic pseudocyst medical condition
liver disease disorder of the human liver
polyuria excessive or abnormally large production or passage of urine
Pit rosea small.jpg
pityriasis rosea type of skin rash
cor pulmonale human disease
mitral valve stenosis mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart
nephronophthisis congenital disorder of urinary system
vascular disease cardiovascular system disease that primarily affects the blood vessels
reperfusion injury tissue damage caused when blood supply returns to the tissue after a period of ischemia or lack of oxygen (anoxia, hypoxia)
polyneuropathy peripheral system disease that is characterized by damage affecting peripheral nerves (peripheral neuropathy) in roughly the same areas on both sides of the body, featuring weakness, numbness, pins-and-needles, and burning pain
limb-girdle muscular dystrophy muscular dystrophy characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles
lupus nephritis inflammation of the kidneys
tricuspid insufficiency A tricuspid valve disease that is characterized by failure of the heart's tricuspid valve to close properly during systole. As a result, with each heart beat, blood is pumped out from the right side of the heart in the opposite direction to normal.
respiratory alkalosis Respiratory alkalosis is a medical condition in which increased respiration reduces the arterial levels of carbon dioxide that, in turn, elevates the blood pH beyond the normal range (7.35-7.45)
rib fracture break in a rib bone
nephritic syndrome medical condition with the kidneys
pulmonary atresia medical condition
Miller–Dieker lissencephaly syndrome A syndrome characterized by classical lissencephaly and distinct facial features. Visible and submicroscopic deletions of 17p13.3, including the LIS1 gene, are found in almost 100% of patients.
neuromuscular disease neuropathy that affect the nerves that control the voluntary muscles
Vancomycin-resistant Staphylococcus aureus Antibiotica resistant bacteria
Vancomycin-resistant Enterococcus
protein S deficiency disorder associated with increased risk of venous thrombosis
Nezelof syndrome Human disease
non-small-cell lung carcinoma type of tumour
Diagram of the human heart (cropped).svg
pulmonary valve insufficiency disease that occurs when the pulmonary valve is not strong enough to prevent backflow into the right ventricle
kidney papillary necrosis Human disease
rhizomelic chondrodysplasia punctata Human disease
ulnar neuropathy Human disease
Post-Ebola virus syndrome Sequelae following recovery from Ebola virus disease

abnormally high value[edit]

image Article description instance of
portal hypertension hypertension in the hepatic portal system abnormally high value
Illu pulmonary circuit.jpg
pulmonary hypertension hypertension characterized by an increase of blood pressure in the pulmonary artery, pulmonary vein or pulmonary capillaries abnormally high value

cause of death[edit]

image Article description instance of
Purple ribbon.svg
domestic violence pattern of behavior which involves the abuse of one family member by another cause of death
stillbirth death of a fetus before or during delivery, resulting in delivery of a dead baby cause of death
health problem
Pneumonia, mixed patterns, lobar and bronchopneumonia (3679096639).jpg
pneumonia inflammatory condition of the lung cause of death
infectious disease

designated intractable/rare diseases[edit]

image Article description instance of
ALS Coronal.jpg
amyotrophic lateral sclerosis neurodegenerative disease characterized by progressive muscular paralysis designated intractable/rare diseases
rare disease
dermatomyositis myositis that results in inflammation located in muscle or located in skin where a skin rash is often seen prior to the onset of muscle weakness designated intractable/rare diseases
BOR Syndrome4.JPG
branchiootorenal syndrome autosomal dominant genetic disorder involving the kidneys, ears, and neck designated intractable/rare diseases
rare disease
congenital dyserythropoietic anemia congenital hemolytic anemia characterized by ineffective erythropoiesis, and resulting from a decrease in the number of red blood cells (RBCs) in the body and a less than normal quantity of hemoglobin in the blood designated intractable/rare diseases
rare disease
Early neurofibromatosis.jpg
neurofibromatoses human diseases designated intractable/rare diseases
rare disease
muscular dystrophy diseases that weaken the body's muscles designated intractable/rare diseases
Crescentic glomerulonephritis (2).jpg
rapidly progressive glomerulonephritis human disease designated intractable/rare diseases
Kennedy disease Kennedy's disease, also known as bulbospinal muscular atrophy (BSMA), is a rare X-linked recessive motor neuron disease characterized by proximal and bulbar muscle wasting designated intractable/rare diseases
rare disease
autosomal dominant familial periodic fever human disease designated intractable/rare diseases
rare disease
Ullrich congenital muscular dystrophy Ullrich congenital muscular dystrophy (UCMD) is characterized by early-onset, generalized and slowly progressive muscle weakness, multiple proximal joint contractures, marked hypermobility of the distal joints and normal intelligence designated intractable/rare diseases
rare disease
autosomal dominant polycystic kidney disease congenital disorder of urinary system designated intractable/rare diseases
pulmonary venoocclusive disease Human disease designated intractable/rare diseases
rare disease
Synapse diag3.png
myasthenia gravis human disease designated intractable/rare diseases

developmental defect during embryogenesis[edit]

image Article description instance of
beta-mannosidosis lysosomal storage disease that has material basis in deficiency of the beta-A-manosidase enzyme resulting in the disruption of N-linked glycoprotein oligosaccharide catabolism developmental defect during embryogenesis
Bannayan-Riley-Ruvalcaba syndrome a rare overgrowth syndrome and hamartomatous disorder with occurrence of multiple subcutaneous lipomas, macrocephaly and hemangiomas. developmental defect during embryogenesis
rare disease
Aortic stenosis rheumatic, gross pathology 20G0014 lores.jpg
aortic valve stenosis aortic valve disease that has physical basis in incomplete opening of the aortic valve developmental defect during embryogenesis
rare disease
Legius syndrome rare genetic skin pigmentation disorder characterized by multiple cafe-au-lait macules developmental defect during embryogenesis
rare disease
acrodermatitis enteropathica Human disease developmental defect during embryogenesis
rare disease
hereditary neuropathy with liability to pressure palsies peripheral neuropathy developmental defect during embryogenesis
Cantú syndrome osteochondrodysplasia characterized by congenital hypertrichosis, neonatal macrosomia, and cardiomegaly developmental defect during embryogenesis
rare disease
Kaufman oculocerebrofacial syndrome . An autosomal recessive mode of inheritance seems most likely. developmental defect during embryogenesis
rare disease
oculocerebrorenal syndrome Human disease developmental defect during embryogenesis
rare disease
lissencephaly Brain disorder that prevents growth of brain folds developmental defect during embryogenesis
designated intractable/rare diseases
rare disease
Ring chromosome 14 syndrome very rare human chromosome abnormality developmental defect during embryogenesis
mulibrey nanism Human disease developmental defect during embryogenesis
rare disease
multicystic dysplastic kidney congenital disorder of urinary system developmental defect during embryogenesis


image Article description instance of
dyslexia neurological condition, developmental or acquired, characterized by trouble with reading despite normal intelligence disease
learning disability
reading disability
hemophilia Human genetic disease that impairs the body's ability to make blood clots, a process needed to stop bleeding disease
umbrella term
rare disease
Hsv encephalitis.jpg
encephalitis acute inflammation of the brain with flu-like symptoms disease
Prefrontal cortex.png
frontal lobe disorder disorder disease
Hyperplasia vs Hypertrophy.svg
hyperplasia increase in the amount of organic tissue that results from cell proliferation disease
hypocalcaemia low calcium levels in blood serum disease
abnormally low value
Nodular glomerulosclerosis.jpeg
diabetic nephropathy disease disease
Hyper IgM syndrome primary immune deficiency disorders characterized by defective CD40 signaling disease
rare disease
chronic pancreatitis human disease disease
beta thalassemia thalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobin disease
rare disease
arterial tortuosity syndrome connective tissue disease that is characterized by elongation and generalized tortuosity of the major arteries including the aorta disease
developmental defect during embryogenesis
rare disease
17-beta-hydroxysteroid dehydrogenase deficiency human disease disease
developmental defect during embryogenesis
rare disease
delta thalassemia type of thalassemia disease
ischemic hepatitis medical condition disease
Jackson–Weiss syndrome disease disease
developmental defect during embryogenesis
fungal sinusitis Inflammation of the paranasal sinuses due to fungal infection disease
Viper bite.jpg
snakebite injury caused by a bite from a snake disease
sepsis life-threatening organ dysfunction triggered by infection disease
Erythema migrans - erythematous rash in Lyme disease - PHIL 9875.jpg
Lyme disease infectious disease caused by Borrelia bacteria, spread by ticks disease
mitral valve insufficiency disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood disease
Polymyositis HE.jpg
polymyositis rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes disease
subacute bacterial endocarditis Human disease disease
infectious disease
Ragged red fibres - gtc - very high mag.jpg
metabolic disease disease that involving errors in metabolic processes of building or degradation of molecules disease
polymicrogyria A condition that affects the development of the human brain by multiple small gyri (microgyri) creating excessive folding of the brain leading to an abnormally thick cortex. disease
renovascular hypertension Human disease disease
platelet storage pool deficiency Human disease disease
Healthy Human T Cell.jpg
T cell deficiency Human disease disease
Anembryonic gestation.jpg
miscarriage natural death of an embryo or fetus before it is able to survive independently disease

genetic disease[edit]

image Article description instance of
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome hypersensitivity reaction type II disease characterized by onset in infancy of refractory diarrhea, endocrinopathies, type 1 diabetes mellitus, and dermatitis that has material basis in mutation in the FOXP3 gene on chromosome Xp11 genetic disease
congenital hyperinsulinism genetic disease genetic disease
Mitochondrial trifunctional protein deficiency medical condition genetic disease
rare disease

infectious disease[edit]

image Article description instance of
Trypanosoma sp. PHIL 613 lores.jpg
African trypanosomiasis parasitic disease infectious disease
cysticercosis Human helminthiasis infectious disease
Hepatitis E virus.jpg
hepatitis E Human disease infectious disease
notifiable disease
Trypanosoma cruzi crithidia.jpeg
Chagas disease human disease infectious disease
Cryptosporidium muris.jpg
cryptosporidiosis Human disease infectious disease
leprosy Chronic infection caused by bacteria Mycobacteria lepræ and lepromatosis infectious disease
Rash of rubella on skin of child's back.JPG
rubella human viral disease infectious disease
notifiable disease
Marburg virus.jpg
Marburg virus disease Human disease infectious disease
Phlebotomus pappatasi bloodmeal finished.jpg
zoonosis pathogenic disease that can be transmitted from one animal species to another (or human) infectious disease
opisthorchiasis Human helminthiasis infectious disease
HAM human disease infectious disease
designated intractable/rare diseases
tuberculous meningitis human disease infectious disease
Alexius Salvador Zika-Virus.jpg
Zika fever infectious arboviral disease infectious disease
Smallpox virus virions TEM PHIL 1849.JPG
smallpox eradicated human disease infectious disease

rare disease[edit]

image Article description instance of
Guillain–Barré Syndrome autoimmune disease that causes the immune system to attack part of the peripheral nervous system rare disease
alpha thalassemia Alpha thalassemia is a thalassemia involving the genes HBA1and HBA2 hemoglobin genes rare disease
Glycogen storage disease in liver - high mag.jpg
glycogen storage disease III human disease rare disease
dysautonomia any disease or malfunction of the autonomic nervous system rare disease
neurological disorder
argininemia urea cycle disorder that involves arginase deficiency resulting in elevated levels of plasma arginine rare disease
hypochondroplasia osteochondrodysplasia that has material basis in mutation in the FGFR3 gene which affects ossification of cartilage and results in short limb dwarfism rare disease
Emery-Dreifuss muscular dystrophy muscular dystrophy that chiefly affects muscles used for movement (skeletal) and heart (cardiac) muscle rare disease
empty sella syndrome endocrine disease rare disease
hemophilia C human disease rare disease
atransferrinemia Human disease rare disease
Fukuyama congenital muscular dystrophy Human disease rare disease
Becker muscular dystrophy X-linked recessive inherited disorder characterized by slowly progressive muscle weakness of the legs and pelvis rare disease
muscular dystrophy
chronic mucocutaneous candidiasis human disease rare disease
autoimmune polyendocrine syndrome type 1 autoimmune polyendocrine syndrome that is inherited in an autosomal recessive fashion, which is characterized by abnormal functioning of the immune system that causes auto-reactivity against endocrine organs rare disease
adenylosuccinase lyase deficiency a rare autosomal recessive metabolic disorder rare disease
Albright's hereditary osteodystrophy osteochondrodysplasia that has material basis in lack of responsiveness to parathyroid hormone which results in shortening and widening of long bones of the located in hand or located in foot along with short stature, obesity, and rounded face rare disease
Cernunnos deficiency Cernunnos-XLF deficiency is a rare form of combined immunodeficiency characterized by microcephaly, growth retardation, and T and B cell lymphopenia rare disease
Bare lymphocyte syndrome 2 human disease rare disease
Auguste D aus Marktbreit.jpg
Alzheimer's disease progressive, neurodegenerative disease characterized by memory loss rare disease
microcephaly medical condition in which the brain does not develop properly resulting in a smaller than normal head rare disease
abnormally low value
Myxomatous aortic valve.jpg
mitral valve prolapse mitral valve disease where one or both of the cusps of the mitral valve bulge or collapse backward in the left atrium during systole rare disease
medullary cystic kidney disease inherited form of cystic kidney disease leading to fibrosis and impaired renal function that is caused by mutations in the UMOD gene, which encodes uromodulin/Tamm-Horsfall mucoprotein rare disease
oculopharyngeal muscular dystrophy Oculopharyngeal muscular dystrophy (OPMD) is an adult-onset progressive myopathy characterized by progressive eyelid ptosis, dysphagia, dysarthria and proximal limb weakness rare disease
Pyruvate kinase deficiency congenital nonspherocytic hemolytic anemia that has material basis in homozygous or compound heterozygous mutation in the PKLR gene on chromosome 1q22 rare disease
short-chain acyl-coenzyme A dehydrogenase deficiency lipid metabolism disorder that is characterized by deficiency of the enzyme short chain acyl-CoA dehydrogenase that results in the inability to convert short chain fatty acids rare disease


image Article description instance of
Immunohistochemical detection of Helicobacter pylori histopathology.jpg
Helicobacter pylori species of bacteria taxon
Primary Laos2.jpg
attention deficit hyperactivity disorder range of neurodevelopmental conditions behavioral disorder
Idiopathic cardiomyopathy, gross pathology 20G0018 lores.jpg
cardiomyopathy heart disease and a myopathy that is characterised by deterioration of the function of the heart muscle clinical sign
grief reaction to loss of someone or something close or important negative emotion
COVID-19 respiratory syndrome and infectious disease in humans, caused by SARS coronavirus 2 emerging communicable disease
atypical pneumonia
psychotherapy clinically applied psychology for desired behavior change specialty
Transverse myelitis MRI.jpg
transverse myelitis an inflammatory demyelinating disorder of the spinal cord, either idiopathic or secondary to a known cause physiological condition
thrombocytopenia blood platelet disease characterized by a low platelet count abnormally low value
rare disease
suicidal ideation having an unusual preoccupation with suicide symptom
Giant cell tumor of tendon sheath histopathology(1).jpg
Giant-cell tumor of the tendon sheath Human disease benign neoplasm
Polyposis nasi 1.jpg
nasal polyps polypoidal masses head and neck disease
remdesivir chemical compound chemical compound
antiviral drug
Coronavirus. SARS-CoV-2.png
SARS-CoV-2 strain of virus causing the ongoing pandemic of coronavirus disease 2019 (COVID-19) group or class of strains
Histopathology of malaria exoerythrocytic forms in liver 07G0024 lores.jpg
malaria mosquito-borne infectious disease endemic disease
tuberculosis infectious disease caused by the bacterium Mycobacterium tuberculosis notifiable disease
endemic disease
schizophrenia psychotic disorder characterized by emotional responsiveness and disintegration of thought process mental disorder

∑ 194 items.

End of automatically generated list.