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.

Table[edit]

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 "en.wikipedia.org" . 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


[edit]

image Article description instance of
coma state of unconsciousness
anosmia the inability to smell
Vestibulocerebellar syndrome medical condition
fat embolism type of embolism
hepatomegaly symptom
autosomal recessive polycystic kidney recessive form of polycystic kidney disease
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
Idiopathic sclerosing mesenteritis medical condition
Snellen chart.svg
Childhood blindness medical condition
Sputum.JPG
sputum mucus that is coughed up from the lower airways
pancreatic pseudocyst medical condition
polyuria excessive or abnormally large production or passage of urine
reperfusion injury tissue damage caused when blood supply returns to the tissue after a period of ischemia or lack of oxygen (anoxia, hypoxia)
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)
Fracturedribsmarked.jpg
rib fracture break in a rib bone
nephritic syndrome medical condition with the kidneys
pulmonary atresia medical condition
Vancomycin-resistant Staphylococcus aureus Antibiotica resistant bacteria
Vancomycin-resistant Enterococcus antibiotic-resistant microorganism
Post-Ebola virus syndrome Sequelae following recovery from Ebola virus disease


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
crime
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
disease (class)


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
disease (class)
XRaydermatomyositis.jpg
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
disease (class)
BOR Syndrome4.JPG
branchiootorenal syndrome autosomal dominant genetic disorder involving the kidneys, ears, and neck designated intractable/rare diseases
rare disease
disease (class)
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
disease (class)
Early neurofibromatosis.jpg
neurofibromatoses human diseases designated intractable/rare diseases
rare disease
disease (class)
muscular dystrophy diseases that weaken the body's muscles designated intractable/rare diseases
disease (class)
Crescentic glomerulonephritis (2).jpg
rapidly progressive glomerulonephritis human disease designated intractable/rare diseases
disease (class)
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
disease (class)
autosomal dominant familial periodic fever human disease designated intractable/rare diseases
rare disease
disease (class)
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
disease (class)
autosomal dominant polycystic kidney disease congenital disorder of urinary system designated intractable/rare diseases
disease (class)
pulmonary venoocclusive disease Human disease designated intractable/rare diseases
rare disease
disease (class)
Synapse diag3.png
myasthenia gravis human disease designated intractable/rare diseases
disease (class)


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
disease (class)
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
disease (class)
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
disease (class)
Legius syndrome rare genetic skin pigmentation disorder characterized by multiple cafe-au-lait macules developmental defect during embryogenesis
rare disease
disease
acrodermatitis enteropathica Human disease developmental defect during embryogenesis
rare disease
disease (class)
hereditary neuropathy with liability to pressure palsies peripheral neuropathy developmental defect during embryogenesis
disease (class)
Cantú syndrome osteochondrodysplasia characterized by congenital hypertrichosis, neonatal macrosomia, and cardiomegaly developmental defect during embryogenesis
rare disease
disease (class)
Kaufman oculocerebrofacial syndrome . An autosomal recessive mode of inheritance seems most likely. developmental defect during embryogenesis
rare disease
disease
disease (class)
oculocerebrorenal syndrome Human disease developmental defect during embryogenesis
rare disease
disease (class)
lissencephaly Brain disorder that prevents growth of brain folds developmental defect during embryogenesis
designated intractable/rare diseases
rare disease
disease (class)
Ring chromosome 14 syndrome very rare human chromosome abnormality developmental defect during embryogenesis
mulibrey nanism Human disease developmental defect during embryogenesis
rare disease
disease (class)
multicystic dysplastic kidney congenital disorder of urinary system developmental defect during embryogenesis


disease[edit]

image Article description instance of
Writing Systems Template Image.svg
dyslexia neurological condition, developmental or acquired, characterized by trouble with reading despite normal intelligence disease
learning disability
reading disability
disease (class)
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
disease (class)
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
disease (class)
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
disease (class)
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
disease (class)
17-beta-hydroxysteroid dehydrogenase deficiency human disease disease
developmental defect during embryogenesis
rare disease
delta thalassemia type of thalassemia disease
disease (class)
ischemic hepatitis medical condition disease
Jackson–Weiss syndrome disease disease
developmental defect during embryogenesis
disease (class)
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
symptom
Erythema migrans - erythematous rash in Lyme disease - PHIL 9875.jpg
Lyme disease infectious disease caused by Borrelia bacteria, spread by ticks disease
disease (class)
mitral valve insufficiency disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood disease
disease (class)
Polymyositis HE.jpg
polymyositis rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes disease
disease (class)
subacute bacterial endocarditis Human disease disease
infectious disease
disease (class)
Ragged red fibres - gtc - very high mag.jpg
metabolic disease disease that involving errors in metabolic processes of building or degradation of molecules disease
disease (class)
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
disease (class)
platelet storage pool deficiency Human disease disease
disease (class)
Healthy Human T Cell.jpg
T cell deficiency Human disease disease
disease (class)
Anembryonic gestation.jpg
miscarriage natural death of an embryo or fetus before it is able to survive independently disease


disease (class)[edit]

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 disease (class)
ERCP cholangioca.jpg
cholangiocarcinoma bile duct adenocarcinoma that has material basis in bile duct epithelial cells. disease (class)
Hypermetropia.svg
hyperopia visual defect which causes to see the far objects clearly and near objects unclearly disease (class)
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 disease (class)
eclampsia pre-eclampsia characterized by the presence of seizures disease (class)
Cholangitis.jpg
cholangitis bile duct disease that is an inflammation of the bile duct disease (class)
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 disease (class)
autoimmune polyendocrine syndrome autoimmune disease of endocrine system with auto-reactivity against endocrine organs disease (class)
Bernard-Soulier syndrome Human disease disease (class)
congenital muscular dystrophy human disease disease (class)
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. disease (class)
acute proliferative glomerulonephritis Human disease disease (class)
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 disease (class)
Haemophilus parainfluenzae Endocarditis PHIL 851 lores.jpg
infective endocarditis endocarditis that is characterized by inflammation of the endocardium caused by infectious agents. disease (class)
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. disease (class)
1471-2415-12-28-1Cerebral angiogram.jpg
cerebrovascular disease artery disease that is characterized by dysfunction of the blood vessels supplying the brain disease (class)
constrictive pericarditis heart disorder in which the pericardial sac becomes thickened and fibrotic, tightening the myocardium and impeding the normal myocardial function disease (class)
hemopericardium pericardial effusion that results from blood in the pericardial sac disease (class)
hyperpituitarism endocrine disease disease (class)
Cytomegalovirus retinitis retinitis that has material basis in Cytomegalovirus disease (class)
Skin Tumors-010.jpg
acral lentiginous melanoma kind of lentiginous skin melanoma disease (class)
Buschke–Ollendorff syndrome medical condition disease (class)
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 disease (class)
Endothelial dysfunction Atherosclerosis.png
atherosclerosis form of arteriosclerosis disease (class)
glycogen storage disease IX glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity disease (class)
Autosomal dominant - en.svg
Activated PI3K Delta Syndrome medical condition disease (class)
Symptoms of leukemia.png
leukemia group of cancers that usually begin in the bone marrow disease (class)
Blue circle for diabetes.svg
type-1 diabetes form of diabetes mellitus disease (class)
Gray591.png
portal hypertension hypertension in the hepatic portal system disease (class)
protein-losing enteropathy Human disease disease (class)
thrombophlebitis phlebitis that results from a blood clot in the vessel disease (class)
radial neuropathy Human disease disease (class)
Стеноз ниркової артерії.jpg
renal artery obstruction narrowing of one of the renal arteries, most often caused by atherosclerosis or fibromuscular dysplasia disease (class)
pulmonary valve stenosis Human disease disease (class)
liver disease disorder of the human liver disease (class)
Pit rosea small.jpg
pityriasis rosea type of skin rash disease (class)
Illu pulmonary circuit.jpg
pulmonary hypertension medical condition disease (class)
cor pulmonale human disease disease (class)
mitral valve stenosis mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart disease (class)
nephronophthisis congenital disorder of urinary system disease (class)
vascular disease cardiovascular system disease that primarily affects the blood vessels disease (class)
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 disease (class)
limb-girdle muscular dystrophy muscular dystrophy characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles disease (class)
lupus nephritis inflammation of the kidneys disease (class)
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. disease (class)
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. disease (class)
neuromuscular disease neuropathy that affect the nerves that control the voluntary muscles disease (class)
protein S deficiency disorder associated with increased risk of venous thrombosis disease (class)
Nezelof syndrome Human disease disease (class)
non-small-cell lung carcinoma any type of epithelial lung cancer other than small-cell lung carcinoma disease (class)
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 disease (class)
kidney papillary necrosis Human disease disease (class)
rhizomelic chondrodysplasia punctata Human disease disease (class)
ulnar neuropathy Human disease disease (class)


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
syndrome
disease (class)
congenital hyperinsulinism genetic disease genetic disease
Mitochondrial trifunctional protein deficiency medical condition genetic disease
rare disease
disease
disease (class)


infectious disease[edit]

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


rare disease[edit]

image Article description instance of
Guillain-barré syndrome - Nerve Damage.gif
Guillain–Barré Syndrome autoimmune disease that causes the immune system to attack part of the peripheral nervous system rare disease
disease (class)
alpha thalassemia Alpha thalassemia is a thalassemia involving the genes HBA1and HBA2 hemoglobin genes rare disease
disease (class)
Glycogen storage disease in liver - high mag.jpg
glycogen storage disease III human disease rare disease
disease (class)
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
disease (class)
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
disease (class)
Emery-Dreifuss muscular dystrophy muscular dystrophy that chiefly affects muscles used for movement (skeletal) and heart (cardiac) muscle rare disease
disease (class)
empty sella syndrome endocrine disease rare disease
disease (class)
hemophilia C human disease rare disease
disease (class)
atransferrinemia Human disease rare disease
disease (class)
Fukuyama congenital muscular dystrophy Human disease rare disease
disease (class)
Becker muscular dystrophy X-linked recessive inherited disorder characterized by slowly progressive muscle weakness of the legs and pelvis rare disease
muscular dystrophy
disease (class)
chronic mucocutaneous candidiasis human disease rare disease
disease (class)
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
disease (class)
adenylosuccinase lyase deficiency a rare autosomal recessive metabolic disorder rare disease
disease (class)
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
disease
disease (class)
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
disease
Bare lymphocyte syndrome 2 human disease rare disease
disease
disease (class)
Auguste D aus Marktbreit.jpg
Alzheimer's disease progressive, neurodegenerative disease characterized by memory loss rare disease
disease (class)
Microcephaly.png
microcephaly medical condition in which the brain does not develop properly resulting in a smaller than normal head rare disease
disease (class)
thrombocytopenia blood platelet disease characterized by a low platelet count rare disease
disease (class)
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
disease (class)
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
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
disease (class)
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
disease (class)
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
disease (class)


Misc[edit]

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
disability
disease (class)
Caesarian.jpg
cesarean section surgical procedure in which a baby is delivered through a mother's abdomen medical procedure
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
disease (class)
Evstafiev-bosnia-sarajevo-funeral-reaction.jpg
grief reaction to loss of someone or something close or important negative emotion
Fphar-11-00937-g001.jpg
COVID-19 respiratory syndrome and infectious disease in humans, caused by SARS coronavirus 2 emerging communicable disease
atypical pneumonia
disease (class)
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
disease (class)
Albert Lefeuvre - Apres le travail.jpg
occupational burnout type of work-related stress, with symptoms characterized by feelings of energy depletion or exhaustion; increased mental distance from one’s job, or feelings of negativism or cynicism related to one's job; and reduced professional efficacy syndrome
Diffuse proliferative lupus nephritis.jpg
nephritis inflammation of the kidneys Wikimedia disambiguation page
disease (class)
suicidal ideation having an unusual preoccupation with suicide symptom
disease
Giant cell tumor of tendon sheath histopathology(1).jpg
Giant-cell tumor of the tendon sheath Human disease benign neoplasm
disease (class)
Polyposis nasi 1.jpg
nasal polyps polypoidal masses head and neck disease
SARS-CoV-2 without background.png
SARS-CoV-2 virus that causes COVID-19 group or class of strains
strain
Histopathology of malaria exoerythrocytic forms in liver 07G0024 lores.jpg
malaria mosquito-borne infectious disease endemic disease
disease (class)
Tuberculosis-x-ray-1.jpg
tuberculosis infectious disease caused by the bacterium Mycobacterium tuberculosis notifiable disease
endemic disease
disease (class)
schizophrenia psychotic disorder characterized by emotional responsiveness and disintegration of thought process mental disorder
disease (class)

∑ 194 items.

End of automatically generated list.