Wikidata:WikiCite/Wikidata lists/Usage of Scholia in Template Medical resources on the English Wikipedia

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]

Manually update list

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

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
	zoonosis	infectious disease that can be transmitted from one animal species to another (or human)
	stillbirth	death of a fetus before or during delivery, resulting in delivery of a dead baby
	pyonephrosis	infection of the renal collecting system
	reperfusion injury	tissue damage caused when blood supply returns to the tissue after a period of ischemia or lack of oxygen (anoxia, hypoxia)
	Zygoma fracture	form of facial fracture
	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
	pulmonary atresia	medical condition
	Pseudoallergy	intolerance reaction
	vancomycin-resistant Staphylococcus aureus	antibiotic-resistant bacterial strain
	radiation colitis	medical condition
	Vancomycin-resistant Enterococcus	antibiotic-resistant microorganism
	Sclerema neonatorum	medical condition
	Postinflammatory hypopigmentation	medical condition
	Pressure alopecia	medical condition
	Pressure urticaria	medical condition
	Pterygium inversum unguis	medical condition
	Red lunulae	medical condition
	Rheumatoid neutrophilic dermatitis	medical condition
	Rheumatoid vasculitis	medical condition
	Rheumatoid nodulosis	medical condition
	Riga–Fede disease	medical condition
	Self-healing juvenile cutaneous mucinosis	medical condition
	Spotted lunulae	medical condition
	Traumatic anserine folliculosis	medical condition
	Trichostasis spinulosa	medical condition
	Trigeminal trophic lesion	medical condition
	Zahn infarct	pseudo-infarction of the liver
	Preureteric vena cava	congenital disorder of urinary system
	recurrent palmoplantar hidradenitis	medical condition
	Post-Ebola virus syndrome	Sequelae following recovery from Ebola virus disease
	pulmonary vein stenosis	medical condition
	Twiddler's syndrome	medical condition
	Salivary gland aplasia	medical condition
	annuloaortic ectasia	dilation of the proximal ascending aorta and aortic annulus
	atresia	condition in which an orifice or passage in the body is closed or absent
	Achard–Thiers syndrome	Achard–Thiers syndrome combines the features of adrenogenital syndrome and Cushing syndrome. It occurs mainly in post-menopausal women
	oedema glottidis	medical condition
	Balanitis plasmacellularis	medical condition
	Angioleiomyoma	medical condition
	Amyand's hernia	A hernia including the appendix
	Abscess of thymus	medical condition
	Acquired progressive lymphangioma	Human disease
	Acral fibrokeratoma	medical condition
	Actinic granuloma	medical condition
	Acute hemorrhagic edema of infancy	medical condition
	Allopurinol hypersensitivity syndrome	medical condition
	amoebic brain abscess	Human disease
	Annular elastolytic giant-cell granuloma	medical condition
	Annular erythema of infancy	medical condition
	aortocaval compression syndrome	medical condition
	Apocrine nevus	medical condition
	Atrophia maculosa varioliformis cutis	human disease
	Autoimmune progesterone dermatitis	medical condition
	Balloon cell nevus	Human disease
	Myomatous erythrocytosis syndrome	medical condition
	alopecia neoplastica	cutaneous metastatic disease in the scalp
	pancreaticobiliary maljunction	group of anatomical variations of the bile ducts
	Encapsulating peritoneal sclerosis	medical condition
	Amiodarone induced thyrotoxicosis	form of hyperthyroidism
	3p deletion syndrome	medical condition
	10q26 deletion	medical condition
	pancreatic pseudocyst	medical condition
	Megaureter	congenital disorder of urinary system
	nephritic syndrome	medical condition with the kidneys
	Necrospermia	A serious masculine fertility issue.
	Oropharyngeal dysphagia	Difficulty controlling the mouth or throat for swallowing
	abdominal migraine	disorder primarily of children which presents with episodes of abdominal pain without an accompanying headache
	Maydl's hernia	A hernia in the form of W
	Megarectum	medical condition
	Minimal mesangial glomerulonephritis	medical condition
	Mucinous nevus	medical condition
	Multifocal fibrosclerosis	human disease
	Multiple minute digitate hyperkeratosis	medical condition
	Neutrophilic dermatosis of the dorsal hands	medical condition
	odynorgasmia	pain during or following ejaculation
	Osteoma cutis	medical condition
	palisaded neutrophilic and granulomatous dermatitis	connective tissue disease
	perforating granuloma annulare	skin condition
	Pincer nails	medical condition
	Pityriasis lichenoides	medical condition
	Plica neuropathica	medical condition for hair
	Polypoid melanoma	medical condition
	Median palatal cyst	medical condition
	Parakeratosis pustulosa	medical condition
	Pneumoscrotum	medical condition
	Killian–Jamieson diverticulum	medical condition
	Hepatolithiasis	medical condition
	Granulosis rubra nasi	human disease
	Bullous drug reaction	medical condition
	chronic functional abdominal pain	medical condition
	Generalized granuloma annulare	medical condition
	Giant-cell fibroma	type of fibroma
	Giant solitary trichoepithelioma	medical condition
	Granular parakeratosis	cutaneous condition
	Granuloma multiforme	medical condition
	Granuloma gluteale infantum	medical condition
	Hair casts	medical condition
	half and half nails	medical condition
	Hapalonychia	medical condition
	Hepatitis X	medical condition
	Holdsworth fracture	unstable fracture dislocation of the thoraco lumbar junction of the spine
	Hook nail	medical condition
	Humoral immune deficiency	medical condition
	Hyperkeratinization	a disorder of the cells lining the inside of a hair follicle
	Idiopathic facial aseptic granuloma	skin condition
	Inappropriate sinus tachycardia	rare type of cardiac arrhythmia, within the category of supraventricular tachycardia
	Juvenile plantar dermatosis	medical condition
	Leukemia cutis	medical condition
	lichen spinulosus	medical condition
	Lipedematous alopecia	medical condition
	ischemic cardiomyopathy	type of cardiomyopathy caused by a narrowing of the coronary arteries which supply blood to the heart
	Glenolabral articular disruption	Shoulder injury
	Hypertrichosis cubiti	medical condition
	Idiopathic granulomatous hepatitis	medical condition
	High-arched palate	Congenital anomaly
	intraarticular fracture	medical condition
	Granular myringitis	medical condition
	Ischemic monomelic neuropathy	human disease
	Lace bite	sports injury
	basophilia	medical condition
	Bile duct hamartoma	congenital disorder of digestive system
	basaloid follicular hamartoma	benign tumor
	Bifascicular block	conduction abnormality in the heart
	Bosworth fracture	ankle fracture
	Bromoderma	medical condition
	cylindroma	medical condition
	fat embolism	type of embolism
	chondrodermatitis nodularis chronica helicis	medical condition
	enteropathic arthropathy	medical condition
	Cryptotia	human disease
	Factitious dermatitis	self-inflicted injuries designed to mimic dermatitis
	calcinosis cutis	medical condition in which calcium deposits form in the skin
	collagenous fibroma	benign fibrous tumor
	Congenital erosive and vesicular dermatosis	medical condition
	Cranioschisis	Neural tube defect in which the brain is exposed
	Cutaneous ciliated cyst	medical condition
	Cutaneous perforating disorders	medical condition
	Desmoplastic trichoepithelioma	medical condition
	Disseminate and recurrent infundibulofolliculitis	medical condition
	Drug-induced pruritus	medical condition
	Dysacusis	Hearing impairment and discomfort due a distorted perception of sound
	Eccrine nevus	medical condition
	Endocapillary proliferative glomerulonephritis	medical condition
	Erythromelanosis follicularis faciei et colli	medical condition
	fibrosing colonopathy	medical condition
	Focal proliferative nephritis	medical condition
	folliculosebaceous cystic hamartoma	medical condition
	Cord colitis syndrome	medical condition
	Eosinophilic cystitis	medical condition
	Childhood blindness	medical condition
	Collagen-induced arthritis	medical condition
	epididymal cyst	medical condition
	Frictional alopecia	dermatological condition
	Ejaculation disorders	most common sexual dysfunction in men
	Congenital athymia	rare immune disorder where the thymus is missing at birth

class of disease[edit]

Article	description	instance of
snakebite	injury caused by a bite from a snake	class of disease
type-1 diabetes	form of diabetes mellitus	class of disease symptom or sign
prosopagnosia	inability to recognize familiar faces	class of disease
protein-losing enteropathy	Human disease	class of disease
thrombophlebitis	phlebitis that results from a blood clot in the vessel	class of disease symptom or sign
radial neuropathy	Human disease	class of disease
renal artery obstruction	narrowing of one of the renal arteries, most often caused by atherosclerosis or fibromuscular dysplasia	class of disease
pulmonary valve stenosis	Human disease	class of disease
pulmonary hypertension	medical condition	class of disease symptom or sign
cor pulmonale	human disease	class of disease
vascular disease	cardiovascular system disease that primarily affects the blood vessels	class of disease
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.	class of disease
arrhythmogenic right ventricular dysplasia 1	arrhythmogenic right ventricular dysplasia that has material basis in heterozygous mutation in the TGFB3 gene on chromosome 14q24	class of disease
protein S deficiency	disorder associated with increased risk of venous thrombosis	class of disease
Tumid lupus erythematosus	medical condition	class of disease
renovascular hypertension	Human disease	class of disease
Pseudopelade of Brocq	medical condition	class of disease
pulmonary valve insufficiency	disease that occurs when the pulmonary valve is not strong enough to prevent backflow into the right ventricle	class of disease
49,XXXXY	The 49,XXXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of three extra X chromosomes in males	class of disease
Progressive nodular histiocytosis	medical condition	class of disease
kidney papillary necrosis	Human disease	class of disease
rhizomelic chondrodysplasia punctata	Human disease	class of disease
subacute cutaneous lupus erythematosus	medical condition	class of disease
T cell deficiency	Human disease	class of disease
ulnar neuropathy	Human disease	class of disease
Uremic pruritus	medical condition	class of disease
ascending cholangitis	bile duct disease that is an inflammation of the bile duct	class of disease symptom or sign
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	class of disease
Vestibulocerebellar syndrome	medical condition	class of disease
autoimmune polyendocrine syndrome	autoimmune disease of endocrine system with auto-reactivity against endocrine organs	class of disease
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.	class of disease
acute proliferative glomerulonephritis	Human disease	class of disease
autosomal recessive polycystic kidney	recessive form of polycystic kidney disease	class of disease
Anetoderma	Primary anetoderma is a rare skin disease characterized by loss of elastin tissue resulting in localized areas of flaccid skin in the absence of a secondary cause	class of disease
adrenal crisis	medical emergency	class of disease
acral lentiginous melanoma	kind of lentiginous skin melanoma	class of disease
Acral persistent papular mucinosis	medical condition	class of disease
adrenal gland disease	endocrine disease	class of disease
aggressive digital papillary adenocarcinoma	medical condition	class of disease
follicular mucinosis	Human disease	class of disease
amelanotic melanoma	human disease	class of disease
angiolipoma	lipoma that is a painful subcutaneous nodule, having all other features of a typical lipoma	class of disease
skin epithelioid hemangioma	Human disease	class of disease
angioma serpiginosum	skin hemangioma characterized by the presence of small red dots that cluster together to form a linear or snake-like array or ring-shaped pattern located in the blood vessels of the skin	class of disease
anorectal anomalies	human disease	class of disease
antisynthetase syndrome	human disease	class of disease
aponeurotic fibroma	human disease	class of disease
atherosclerosis	human disease	class of disease
autoimmune encephalitis	type of encephalitis	class of disease
achondrogenesis type IB	achondrogenesis that has material basis in mutation in the SLC26A2 gene which results in umbilical or inguinal hernia and a prominent rounded abdomen	class of disease
achondrogenesis type II	achondrogenesis that has material basis in mutations in the COL2A1 gene which results in underdeveloped lungs, hydrops fetalis, a prominent forehead and abnormal ossification of the located in vertebral column or located in pelvis	class of disease
autoimmune enteropathy	medical condition	class of disease
Autoimmune polyendocrine syndrome type 3	human disease	class of disease
activated PI3K delta syndrome	medical condition	class of disease
Anti-IgLON5 disease	human disease	class of disease
acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome	This syndrome is characterised by the association of acanthosis nigricans, insulin resistance, severe muscle cramps and acral hypertrophy	class of disease
15q overgrowth syndrome	human disease	class of disease
chronic spontaneous urticaria	human disease	class of disease
oromandibular dystonia	focal dystonia that is characterized by distortions of the mouth and tongue.	class of disease
portal hypertension	hypertension in the hepatic portal system	class of disease
mitral valve insufficiency	disorder of the heart in which the mitral valve does not close properly when the heart pumps out blood	class of disease
Aagenaes syndrome	syndrome that is characterized by congenital hypoplasia of lymph vessels, which causes lymphedema of the legs and recurrent cholestasis in infancy, and slow progress to hepatic cirrhosis and giant cell hepatitis with fibrosis of the portal tracts	class of disease
nephritis	inflammation of the kidneys	class of disease symptom or sign
methemoglobinemia	a form of toxic anemia characterized by the presence of methemoglobin in the blood	class of disease
polymyositis	rare idiopathic inflammatory myopathy characterized by symmetric proximal muscle weakness and elevated muscle enzymes	class of disease symptom or sign
pityriasis rosea	type of skin rash	class of disease symptom or sign
mitral valve stenosis	mitral valve disease that is characterized by the narrowing of the orifice of the mitral valve of the heart	class of disease
nephronophthisis	congenital disorder of urinary system	class of disease
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	class of disease
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.	class of disease symptom or sign
neuromuscular disease	neuropathy that affect the nerves that control the voluntary muscles	class of disease
metabolic disease	disease that involving errors in metabolic processes of building or degradation of molecules	class of 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.	class of disease
Marburg multiple sclerosis	human disease	class of disease
Nezelof syndrome	Human disease	class of disease
non-small-cell lung carcinoma	any type of epithelial lung cancer other than small-cell lung carcinoma	class of disease
3-hydroxy-3-methylglutaryl-CoA lyase deficiency	medical condition	class of disease
3 hydroxyisobutyric aciduria	medical condition	class of disease
malignant acrospiroma	Human disease	class of disease
skin pilomatrix carcinoma	Human disease	class of disease
Necrolytic acral erythema	medical condition	class of disease
Onychomatricoma	neoplasm involving a UBERON:0002283	class of disease
Pagetoid reticulosis	medical condition	class of disease
Pemphigus erythematosus	human disease	class of disease
pigmentation disorder	human or animal skin condition	class of disease
Pili annulati	medical condition	class of disease
Pili bifurcati	medical condition	class of disease
pili torti	medical condition	class of disease
platelet storage pool deficiency	Human disease	class of disease
Nodular lichen myxedematosus	medical condition	class of disease
Mouth and genital ulcers with inflamed cartilage syndrome	human disease	class of disease
Pineocytoma	medical condition	class of disease
liver disease	disorder of the human liver	class of disease
gastroparesis	Human disease	class of disease
limb-girdle muscular dystrophy	muscular dystrophy characterized by weakening of the muscles of the hip and shoulders which comprise the limb girdle muscles	class of disease
lupus nephritis	inflammation of the kidneys	class of 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	class of disease symptom or sign
infective endocarditis	endocarditis that is characterized by inflammation of the endocardium caused by infectious agents.	class of disease
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.	class of disease
generalized eruptive histiocytoma	human disease	class of disease
hemopericardium	pericardial effusion that results from blood in the pericardial sac	class of disease
Livedoid vasculitis	vasculitis with purpuric ulcers	class of disease
glomerulopathy	disease involving the renal glomerulus	class of disease
ileitis	inflammatory bowel disease characterized by inflammation located in ileum, has symptom diarrhea, has symptom abdominal pain, often in the right lower quadrant, has symptom weight loss	class of disease
hyperpituitarism	endocrine disease	class of disease
Graham-Little syndrome	medical condition	class of disease
Hexokinase deficiency	medical condition	class of disease
hyperprothrombinemia	human disease	class of disease
Indeterminate cell histiocytosis	human disease	class of disease
Intraretinal microvascular abnormalities	medical condition	class of disease
keratosis pilaris atrophicans	human disease	class of disease
linear focal elastosis	human disease	class of disease
Lupus erythematosus panniculitis	A type of lupus erythematosus characterized by deep dermal or subcutaneous nodules, most often on the head, face, or upper arms. It is generally chronic and occurs most often in women between the ages of 20 and 45.	class of disease
Middle East respiratory syndrome	viral respiratory infection in humans and camels	class of disease
glycogen storage disease IX	glycogen storage disease characterized by deficiency of hepatic phosphorylase kinase activity	class of disease
Interstitial granulomatous dermatitis	human disease	class of disease
Idiopathic sclerosing mesenteritis	medical condition	class of disease
Light chain deposition disease	medical condition	class of disease
leukemia	group of cancers that usually begin in the bone marrow	class of disease symptom or sign
Bernard-Soulier syndrome	Human disease	class of disease
benign cephalic histiocytosis	human disease	class of disease
endocarditis	endocardium disease characterized by inflammation of the endocardium of the heart chambers and valves	class of disease symptom or sign
cholangiocarcinoma	bile duct adenocarcinoma that has material basis in bile duct epithelial cells.	class of disease
hyperopia	visual defect which causes to see the far objects clearly and near objects unclearly	class of disease symptom or sign
cerebral amyloid angiopathy	amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes	class of disease
encephalitis	acute inflammation of the brain with flu-like symptoms	class of disease symptom or sign
eclampsia	pre-eclampsia characterized by the presence of seizures	class of disease
cryptophthalmos	congenital abnormality characterized by the presence of a continuous layer of skin extending over the eyeballs and the absence of eyelids and the palpebral fissure	class of disease
congenital muscular dystrophy	human disease	class of disease
congenital fiber-type disproportion	Human disease	class of disease
cystitis cystica	human disease	class of disease
erosive pustular dermatitis of the scalp	characterized by the development of painful pustules, shallow erosions, and crusting on atrophic skin that eventually result in cicatricial alopecia	class of disease
cerebrovascular disease	artery disease that is characterized by dysfunction of the blood vessels supplying the brain	class of disease
constrictive pericarditis	heart disorder in which the pericardial sac becomes thickened and fibrotic, tightening the myocardium and impeding the normal myocardial function	class of disease
epiblepharon	human disease	class of disease
congenital adrenal hyperplasia due to 21-hydroxylase deficiency	medical condition	class of disease
cytomegalovirus retinitis	retinitis that has material basis in Cytomegalovirus	class of disease
Buschke–Ollendorff syndrome	medical condition	class of disease
chondroid lipoma	lipoma that is a deep-seated, firm, yellow tumors that characteristically occur on the legs of women	class of disease
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	class of disease
congenital hemolytic anemia	Human disease	class of disease symptom or sign
congenital hypoplastic anemia	Human disease	class of disease
nonsyndromic congenital nail disorder 7	Human disease	class of disease
congenital smooth muscle hamartoma	medical condition	class of disease
Cornea plana 1	congenital hereditary deformity of the eye surface	class of disease
cutaneous B-cell lymphoma	human disease	class of disease
cutaneous endometriosis	human disease	class of 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.	class of disease
delta thalassemia	type of thalassemia	class of disease
discrete papular lichen myxedematosus	skin condition	class of disease
drug-induced autoimmune hemolytic anemia	Drug-induced autoimmune hemolytic anemia is a type of autoimmune hemolytic anemia (AIHA; see this term) that occurs as a reaction to therapeutic drugs, and can be due to various mechanisms	class of disease
epidermolytic acanthoma	Human disease	class of disease
Familial cirrhosis	congenital disorder of digestive system	class of disease
COACH Syndrome	a rare autosomal recessive disorder characterised by Cerebellar vermis hypoplasia, Oligophrenia (developmental delay/mental retardation), Ataxia, Coloboma, and Hepatic fibrosis.	class of disease

clinical sign[edit]

Article	description	instance of
nephromegaly	abnormally enlarged kidneys	clinical sign
hyperproteinemia	increased concentration of proteins in the blood	clinical sign
hyperspermia	condition in which a male has an abnormally large ejaculate volume	clinical sign
cardiomyopathy	heart disease and a myopathy that is characterised by deterioration of the function of the heart muscle	clinical sign class of disease
claudication	impairment in walking, or pain, discomfort or tiredness in the legs that occurs during walking and is relieved by rest	clinical sign symptom or sign

designated intractable/rare disease[edit]

Article	description	instance of
rapidly progressive glomerulonephritis	human disease	designated intractable/rare disease class of disease
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 disease rare disease class of disease
autosomal dominant familial periodic fever	human disease	designated intractable/rare disease rare disease class of 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 disease rare disease class of disease
pulmonary venoocclusive disease	Human disease	designated intractable/rare disease rare disease class of disease
ankylosing spondylitis	type of arthritis in which there is long term inflammation of the joints of the spine	designated intractable/rare disease class of disease symptom or sign
amyotrophic lateral sclerosis	rare neurodegenerative disease with amyotrophy and progressive paralysis	designated intractable/rare disease rare disease class of disease symptom or sign
neurofibromatoses	human diseases	designated intractable/rare disease rare disease class of disease symptom or sign
muscular dystrophy	diseases that weaken the body's muscles	designated intractable/rare disease class of disease
autosomal dominant polycystic kidney disease	congenital disorder of urinary system	designated intractable/rare disease class of disease
myasthenia gravis	human disease	designated intractable/rare disease class of disease
branchiootorenal syndrome	autosomal dominant genetic disorder involving the kidneys, ears, and neck	designated intractable/rare disease rare disease class of 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 disease class of 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 disease rare disease class of disease

developmental defect during embryogenesis[edit]

Article	description	instance of
Smith-Lemli-Opitz syndrome	an inborn error of cholesterol synthesis, caused by a mutation in the enzyme 7-Dehydrocholesterol reductase	developmental defect during embryogenesis rare disease class of disease
Ring chromosome 14 syndrome	very rare human chromosome abnormality	developmental defect during embryogenesis class of disease
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 class of disease
aortic valve stenosis	aortic valve disease that has physical basis in incomplete opening of the aortic valve	developmental defect during embryogenesis rare disease class of disease
acrodermatitis enteropathica	Human disease	developmental defect during embryogenesis rare disease class of disease
arterial tortuosity syndrome	connective tissue disease that is characterized by elongation and generalized tortuosity of the major arteries including the aorta	developmental defect during embryogenesis rare disease class of disease
acrofrontofacionasal dysostosis	dysostosis characterized by intellectual disability, short stature, hypertelorism, broad notched nasal tip, cleft lip palate, postaxial camptobrachypolysyndactyly, fibular hypoplasia and anomalies of foot structure	developmental defect during embryogenesis class of disease
Ascher's syndrome	medical condition	developmental defect during embryogenesis class of disease
absence deformity of leg-cataract syndrome	medical condition	developmental defect during embryogenesis class of disease
absent tibia-polydactyly-arachnoid cyst syndrome	Tibia absent - polydactyly - arachnoid cyst syndrome is a very rare constellation of multiple anomalies, including absence or hypoplasia of the tibia	developmental defect during embryogenesis class of disease
pulmonary valve agenesis	congenital abnormality	developmental defect during embryogenesis class of disease
oculocerebrorenal syndrome	Human disease	developmental defect during embryogenesis rare disease class of disease
chromosome 1q21.1 duplication syndrome	Human disease	developmental defect during embryogenesis class of disease
chromosome 1p36 deletion syndrome	Human disease	developmental defect during embryogenesis designated intractable/rare disease class of disease
mulibrey nanism	Human disease	developmental defect during embryogenesis rare disease class of disease
17-beta-hydroxysteroid dehydrogenase deficiency	human disease	developmental defect during embryogenesis rare disease class of disease
8p23.1 duplication syndrome	Genetic disorder	developmental defect during embryogenesis class of disease
multicystic dysplastic kidney	congenital disorder of urinary system	developmental defect during embryogenesis class of disease
osteoporosis-pseudoglioma syndrome	Osteoporosis pseudoglioma syndrome is a very rare autosomal recessive disorder characterized by congenital or infancy-onset blindness and severe juvenile-onset osteoporosis and spontaneous fractures	developmental defect during embryogenesis class of disease
Legius syndrome	rare genetic skin pigmentation disorder characterized by multiple cafe-au-lait macules	developmental defect during embryogenesis rare disease class of disease
lissencephaly	Brain disorder that prevents growth of brain folds	developmental defect during embryogenesis designated intractable/rare disease rare disease class of disease symptom or sign
hereditary neuropathy with liability to pressure palsies	peripheral neuropathy	developmental defect during embryogenesis class of disease
Jackson–Weiss syndrome	disease	developmental defect during embryogenesis class of disease
Kaufman oculocerebrofacial syndrome	. An autosomal recessive mode of inheritance seems most likely.	developmental defect during embryogenesis rare disease class of disease
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 class of disease
bronchopulmonary dysplasia	Human disease of premature infants	developmental defect during embryogenesis class of disease
familial isolated deficiency of vitamin E	rare autosomal recessive neurodegenerative disease. Symptoms are similar to those of Friedreich ataxia	developmental defect during embryogenesis rare disease class of disease
Cantú syndrome	osteochondrodysplasia characterized by congenital hypertrichosis, neonatal macrosomia, and cardiomegaly	developmental defect during embryogenesis rare disease class of disease
Distal Trisomy 10q	Distal trisomy of the long arm of chromosome 10 (10q) is characterized by pre- and postnatal growth retardation, a pattern of specific facial features, hypotonia, and developmental and psychomotor delay	developmental defect during embryogenesis class of disease

disease[edit]

Article	description	instance of
sepsis	life-threatening organ dysfunction triggered by infection	disease symptom symptom or sign
reticular erythematous mucinosis	medical condition	disease
Protein contact dermatitis	medical condition	disease
Right atrial enlargement	medical condition	disease
steroid diabetes	insulin and steroid treatment	disease
subcutaneous fat necrosis of the newborn	medical condition	disease
psoriatic erythroderma	medical condition	disease
transplant glomerulopathy	medical condition	disease
Twin Anemia-Polycythemia Sequence	medical condition	disease
septic thrombophlebitis	medical condition	disease
Progressive cardiac conduction defect	medical condition	disease Wikimedia duplicated page
Acquired perforating dermatosis	medical condition	disease
Acinic cell carcinoma of the lung	medical condition	disease
Alezzandrini syndrome	medical condition	disease
Autoimmune autonomic ganglionopathy	medical condition	disease
Median nail dystrophy	medical condition	disease
AIDS-related lymphoma	medical condition	disease
microvascular occlusion	medical condition	disease
Perforating folliculitis	skin condition involving mainly the hairy parts of the extremities	disease
Pneumosinus dilatans	medical condition	disease
Metropathia haemorrhagica	frequent and heavy menstruation	disease
miscarriage	natural death of an embryo or fetus before it is able to survive independently	disease symptom or sign complications of pregnancy
hamartoma	non-cancerous growth, made up of an abnormal mixture of cells and tissues normally found in the area of the body	disease
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
Hair follicle nevus	medical condition	disease
halogenoderma	medical condition	disease
Inverse psoriasis	medical condition	disease
ischemic hepatitis	medical condition	disease
Inflammatory fibroid polyp	medical condition	disease
MBL deficiency	human disease	disease
Irvine–Gass syndrome	medical condition; common cause of visual loss after cataract surgery	disease adverse effect
fungal sinusitis	Inflammation of the paranasal sinuses due to fungal infection	disease
brachymetatarsia	condition in which there is one or more abnormally short or overlapping toes metatarsals	disease
frontal lobe disorder	disorder	disease
dyslalia	speech disorder	disease
diabetic nephropathy	disease	disease
chronic pancreatitis	human disease	disease
ectopic testis	medical condition	disease
Cruveilhier–Baumgarten disease	medical condition	disease
Frontotemporal dementia and parkinsonism linked to chromosome 17	medical condition	disease

genetic disease[edit]

Article	description	instance of
mitochondrial trifunctional protein deficiency	medical condition	genetic disease rare disease class of disease
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 class of disease
congenital hyperinsulinism	genetic disease	genetic disease class of disease

infectious disease[edit]

Article	description	instance of
rubella	human viral disease	infectious disease notifiable disease class of disease symptom or sign
schistosomiasis	human disease	infectious disease class of disease
HAM	human disease	infectious disease designated intractable/rare disease class of disease
subacute bacterial endocarditis	Human disease	infectious disease class of disease
tuberculous meningitis	human disease	infectious disease
Zika fever	infectious arboviral disease	infectious disease class of disease
smallpox	eradicated human disease	infectious disease class of disease symptom or sign
African trypanosomiasis	parasitic disease	infectious disease class of disease
allergic bronchopulmonary aspergillosis	aspergillosis that involves an allergic reaction due to the spores of Aspergillus moulds (A. fumigatus), which colonizes the mucus in the airways causing inflammation	infectious disease class of disease
Marburg virus disease	Human disease	infectious disease class of disease
opisthorchiasis	Human helminthiasis	infectious disease class of disease
pneumonia	inflammation of the alveoli of the lungs	infectious disease class of disease cause of death
Lyme disease	infectious disease caused by Borrelia bacteria, spread by ticks	infectious disease
hepatitis E	an inflammation of the liver caused by infection with the hepatitis E virus	infectious disease notifiable disease class of disease
impetigo herpetiformis	impetigo that is characterized as a form of severe pustular psoriasis occurring in pregnancy	infectious disease class of disease
leprosy	chronic infection caused by bacteria Mycobacteria lepræ and lepromatosis	infectious disease class of disease
Bickerstaff's encephalitis	rare inflammatory brain disease	infectious disease designated intractable/rare disease class of disease
cysticercosis	Human helminthiasis	infectious disease class of disease
Chagas disease	human disease	infectious disease class of disease
cryptosporidiosis	Human disease	infectious disease class of disease

rare disease[edit]

Article	description	instance of
thrombocytopenia	blood platelet disease characterized by a low platelet count	rare disease class of disease symptom or sign
48, XXXX	rare chromosomal disorder with 4 X chromosomes	rare disease chromosomal disease developmental defect during embryogenesis class of 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 class of disease
Rh deficiency syndrome	Human disease	rare disease class of 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 class of disease
alpha thalassemia	Alpha thalassemia is a thalassemia involving the genes HBA1and HBA2 hemoglobin genes	rare disease class of disease
argininemia	urea cycle disorder that involves arginase deficiency resulting in elevated levels of plasma arginine	rare disease class of disease
atransferrinemia	Human disease	rare disease class of disease
apparent mineralocorticoid excess syndrome	Human disease	rare disease class of disease
acatalasia	Human disease	rare disease class of disease
adrenocorticotropic hormone deficiency	hypopituitarrium that is characterized by a decreased or absent production of adrenocorticotropic hormone by the pituitary gland	rare disease class of 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 class of disease
acrokeratosis verruciformis	Human disease	rare disease class of disease
adenine phosphoribosyltransferase deficiency	An amino acid metabolic disorder characterized by the formation 2,8-dihydroxyadenine stones and renal failure secondary to intratubular crystalline precipitation. It has an autosomal recessive inheritance pattern.	rare disease class of disease
adenylosuccinase lyase deficiency	a rare autosomal recessive metabolic disorder	rare disease class of 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 class of disease
alopecia universalis	human disease	rare disease class of disease symptom or sign
Alzheimer's disease	progressive, neurodegenerative disease characterized by memory loss	rare disease class of disease
microcephaly	medical condition in which the brain does not develop properly resulting in a smaller than normal head	rare disease class of disease
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 class of disease
5-alpha-reductase deficiency	medical condition	rare disease class of 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 class of disease
pentasomy X	sex chromosome aneuploidy where a female has three additional X chromosomes	rare disease chromosomal disease developmental defect during embryogenesis class of disease
Ritscher–Schinzel syndrome	developmental malformation syndrome characterized by craniofacial abnormalities, congenital heart defects, and cerebellar brain malformations.	rare disease medical triad class of 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 class of disease
ornithine carbamoyltransferase deficiency	urea cycle disorder that involves a mutated and ineffective form of the enzyme ornithine transcarbamylase	rare disease metabolic syndrome class of disease
2,4 Dienoyl-CoA reductase deficiency	medical condition	rare disease class of disease
2-methylbutyryl-CoA dehydrogenase deficiency	gene (located on chromosome 10q25-26) have been reported in affected patients. Treatment includes carnitine supplementation and a low-protein diet.	rare disease class of disease
3-methylcrotonyl-CoA carboxylase deficiency	Human disease	rare disease class of disease
Guillain–Barré syndrome	autoimmune disease that causes the immune system to attack part of the peripheral nervous system	rare disease class of disease symptom or sign
glycogen storage disease III	human disease	rare disease class of 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 class of disease
hemophilia C	human disease	rare disease class of disease symptom or sign
hyper IgM syndrome	primary immune deficiency disorders characterized by defective CD40 signaling	rare disease class of disease
Fukuyama congenital muscular dystrophy	Human disease	rare disease class of disease
hypereosinophilic syndrome	unexplained chronic eosinophila	rare disease class of disease
Koolen de Vries syndrome	Human disease	rare disease class of disease
isolated growth hormone deficiency	hypopituitarism characterized by abnormally low levels, absence or impaired function of growth hormone in the absence of abnormalities in other pituitary hormones	rare disease class of disease
Becker muscular dystrophy	X-linked recessive inherited disorder characterized by slowly progressive muscle weakness of the legs and pelvis	rare disease class of disease
beta thalassemia	thalassemia characterized by the reduced or absent synthesis of the beta globin chains of hemoglobin	rare disease class of disease
bare lymphocyte syndrome 2	human disease	rare disease class of disease
dysautonomia	any disease or malfunction, mostly of neurogenic origin, of the autonomic nervous system	rare disease neurological disorder
Dejerine–Sottas disease	a rare hereditary neurological disorder characterised by damage to the peripheral nerves and resulting progressive muscle wasting	rare disease class of disease
Emery-Dreifuss muscular dystrophy	muscular dystrophy that chiefly affects muscles used for movement (skeletal) and heart (cardiac) muscle	rare disease class of disease
empty sella syndrome	endocrine disease	rare disease class of disease
chronic mucocutaneous candidiasis	human disease	rare disease class of disease
Cornea plana 2	medical condition	rare disease class of 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 class of disease
Chilblain lupus	Human disease	rare disease class of disease
combined immunodeficiency	primary immunodeficiency disease that involves multiple components of the immune system, including both humoral immunity and cell-mediated immunity	rare disease class of disease
congenital amegakaryocytic thrombocytopenia	thrombocytopenia characterized by a severe reduction in megakaryocyte and platelet numbers that has material basis in homozygous or compound heterozygous mutation in the MPL gene on chromosome 1p34	rare disease class of disease
Cataract-microcornea syndrome	Cataract-microcornea syndrome is characterized by the association of congenital cataract and microcornea without any other systemic anomaly or dysmorphism	rare disease class of disease

symptom[edit]

Article	description	instance of
suicidal ideation	thoughts, ideas, or ruminations about the possibility of ending one's life	symptom disease
acneiform eruption	medical condition	symptom class of disease
centrilobular necrosis	medical condition	symptom
vascular purpura	medical condition	symptom

symptom or sign[edit]

Article	description	instance of
sputum	mucus that is coughed up from the lower airways	symptom or sign
rectorrhagia	rectal bleeding	symptom or sign
abdominal pain	stomach aches	symptom or sign women's disease
anosmia	the inability to smell	symptom or sign
polyuria	excessive or abnormally large production or passage of urine	symptom or sign abnormally high value
hepatomegaly	symptom	symptom or sign
coma	state of unconsciousness	symptom or sign

syndrome[edit]

image	Article	description	instance of
	low anterior resection syndrome	postoperative complication after removal of the rectum	syndrome
	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

Misc[edit]

Article	description	instance of
psychotherapy	clinically applied psychology for desired behavior change	specialty health specialty academic discipline
transverse myelitis	an inflammatory demyelinating disorder of the spinal cord, either idiopathic or secondary to a known cause	physiological condition class of disease
triple X syndrome	presence of an extra X chromosome in each cell of a female	disorder of sex development class of disease
giant-cell tumor of the tendon sheath	Human disease	benign neoplasm class of disease
SARS-CoV-2	virus that causes COVID-19	group or class of strains strain virus species
tuberculosis	infectious disease caused by the bacterium Mycobacterium tuberculosis	notifiable disease endemic disease class of disease
schizophrenia	psychotic disorder characterized by emotional responsiveness and disintegration of thought process	mental disorder class of disease
attention deficit hyperactivity disorder	neurodevelopmental disorder	behavioral disorder disability class of disease neurodevelopmental disorder neurodiversity
acidosis	a process causing increased acidity in the blood and other body tissues	abnormally low value symptom or sign
Atypical fibroxanthoma	medical condition	health problem
Acne necrotica	skin condition	Wikimedia duplicated page
microcyte	cell type	cell type
nasal polyps	polypoidal masses	head and neck disease
Melanonychia	Black or brown pigmentation of nails	human disease
mesomelia	Abnormal shortness of the forearms and lower legs	hereditary disorder
hemophilia	Human genetic disease that impairs the body's ability to make blood clots, a process needed to stop bleeding	umbrella term rare disease class of disease
Helicobacter pylori	species of bacteria	taxon
grief	reaction to loss of someone or something close or important	negative emotion
ineffective erythropoiesis	disease	medical finding
linear IgA bullous dermatosis	Human disease	autoimmune disease class of disease
malaria	mosquito-borne infectious disease	endemic disease class of disease
dyslexia	specific learning disability characterized by troubles with reading	learning disability reading disability class of disease
domestic violence	pattern of behavior which involves the abuse of one family member by another	cause of death crime matter
cesarean section	surgical procedure in which a baby is delivered through a mother's abdomen	medical procedure
dysorthography	medical condition	specific developmental disorder
Electrical alternans	Electrocardiographic phenomenon indicative of fluid in the pericardium	ECG finding
COVID-19	contagious disease caused by SARS-CoV-2	emerging communicable disease atypical pneumonia class of disease