Members |
targetComponentId |
"Morning after" pills given |
Postcoital oral contraceptive given |
"Sniffing the morning air" position |
Sniffing position (finding) |
17-KS measurement |
17-Ketosteroids measurement (procedure) |
17-OHCS measurement, 24H urine |
Measurement of 17-hydroxycorticosteroid in 24 hour urine specimen |
4-Aminosalicylic acid |
Para-aminosalicylic acid |
6-mercaptopurine (6MP) metabolites |
Measurement of mercaptopurine metabolite |
95% distal pancreatectomy |
95 percent distal pancreatectomy (procedure) |
A vulvovaginoplasty procedure described by Williams to create a vaginal canal |
Construction of vagina (procedure) |
ACPC - Anterior colporrhaphy and posterior colpoperineorrhaphy |
Combined anterior and posterior repair of vagina and perineum (procedure) |
ACPCP - Anterior colporrhaphy and posterior colpoperineorrhaphy |
Combined anterior and posterior repair of vagina and perineum (procedure) |
ACS - Anterior tibial compartment syndrome |
Anterior tibial compartment syndrome |
ACVG - Aortocoronary vein graft |
Aortocoronary artery bypass graft with vein graft |
AH type amyloidosis |
A rare, systemic amyloidosis characterized by the aggregation and deposition of amyloid fibrils composed of monoclonal immunoglobulin heavy-chain fragments, usually produced by a plasma cell neoplasm. Amyloid fibrils deposit in various organs, most commonly in the kidneys. It typically affects older patients and clinical presentation includes signs and symptoms of renal dysfunction, sometimes leading to nephrotic syndrome and end stage renal disease. Cardiac, liver and nerves involvement has also been described. |
AIDS-related complex |
syndrome associé au SIDA |
AMC - Arthrogryposis multiplex congenita |
A group of disorders with characteristics of congenital limb contractures manifesting as limitation of movement of multiple limb joints at birth that is usually non-progressive and may include muscle weakness and fibrosis. This disorder is always associated with decreased intrauterine fetal movement, which leads secondarily to the contractures. |
AMC-Arthrogryposis multiplex congenita |
A group of disorders with characteristics of congenital limb contractures manifesting as limitation of movement of multiple limb joints at birth that is usually non-progressive and may include muscle weakness and fibrosis. This disorder is always associated with decreased intrauterine fetal movement, which leads secondarily to the contractures. |
ARC |
syndrome associé au SIDA |
ATN - Acute tubular necrosis |
Acute tubular necrosis |
AVSD - Atrioventricular septal defect |
Acquired atrioventricular septal defect |
AVSD - Atrioventricular septal defect |
Congenital atrioventricular septal defect (disorder) |
Abdomen feels bloated |
Abdominal bloating (finding) |
Abdominal angina |
Abdominal angina |
Abdominal repair of enterocele |
Repair of vaginal enterocele by abdominal approach |
Abdominoanal pull-through |
Abdominoperineal pull-through procedure |
Abdominoperineal pull-through |
Abdominoperineal pull-through procedure |
Abdominoperineal pull-through and proctectomy |
Abdominoperineal pull-through procedure |
Ability to move |
Ability to move |
Ability to perform ADL - activity of daily living |
Ability to perform activity of daily living (observable entity) |
Abnormal feeling |
Feeling abnormal |
Abnormal presence of protein in urine |
Urine protein outside reference range (finding) |
Abnormal sinus tract |
Sinus tract (morphologic abnormality) |
Abnormal ventriculoarterial connection |
Abnormal ventriculoarterial connection |
Abrasion |
Abrasion (disorder) |
Abrasion of teeth secondary to deleterious oral practices |
Abrasion of teeth due to deleterious oral practices |
Abscess of external auditory meatus |
Abscess of external auditory canal |
Absence of external auditory canal |
Absence of ear canal |
Absence of liver |
Absence of liver (finding) |
Absence of teeth |
Absence of teeth (finding) |
Abuse of elderly person |
Elder abuse |
Acacia specific IgE antibody measurement |
Gum arabic specific IgE antibody measurement |
Acarus siro |
Acarus siro (organism) |
Accelerometry |
Accelerometry (procedure) |
Accident |
Accidental event (event) |
Accidental exposure |
Accidental exposure to potentially harmful entity (event) |
Accretions on tooth |
Accretion on tooth (disorder) |
Aching |
Aching sensation quality (qualifier value) |
Acinar cell carcinoma of lung |
Acinar cell carcinoma of lung (disorder) |
Acinar cell carcinoma of oropharynx |
Acinar cell carcinoma of oropharynx |
Acinar cell carcinoma of trachea |
Acinar cell carcinoma of trachea |
Acinic cell tumor |
Acinar cell tumor |
Acinic cell tumour |
Acinar cell tumor |
Acquired atresia of vagina |
Acquired atresia of vagina (disorder) |
Acquired choledochal cyst |
Acquired choledochal cyst (disorder) |
Acquired deformity of lesser toe |
Acquired deformity of lesser toe |
Acquired hypertrophy of tongue |
Acquired hypertrophy of tongue (disorder) |
Acquired obstruction of coronary sinus |
Acquired obstruction of coronary sinus |
Acquired obstruction of femoral vein |
Acquired obstruction of femoral vein (disorder) |
Acquired occlusion of superior caval vein |
Acquired obstruction of coronary sinus |
Acquired right ventricular hypertrophy |
Acquired hypertrophy of right cardiac ventricle |
Acroangiodermatitis |
Benign condition with purple-colored patches, plaques or nodules, usually found bilaterally on the extensor surfaces of the lower extremities and associated with chronic venous insufficiency and arteriovenous malformations. A reactive angiodysplasia of preexisting cutaneous blood vessels that resembles malignant conditions like Kaposi's sarcoma and requires histopathological examination for its diagnosis and differentiation. |
Acrocephalosyndactyly |
Acrocephalosyndactyly |
Acrodermatitis continua of Hallopeau |
Acrodermatitis continua of Hallopeau |
Acrodermatitis perstans |
Acrodermatitis continua of Hallopeau |
Acroencephalosyndactyly |
Acrocephalosyndactyly |
Acropustulosis |
Acrodermatitis continua of Hallopeau |
Actinomyces ericksonii |
Actinomyces ericksonii |
Activity therapy |
Activity therapy (regime/therapy) |
Acute adrenal insufficiency |
A primary adrenal insufficiency caused by a sudden defective production of adrenal steroids (cortisol and aldosterone). It represents an emergency, thus the rapid recognition and prompt therapy are critical for survival even before the diagnosis is made. |
Acute alcohol intoxication |
Acute alcohol intoxication |
Acute alcoholism |
Acute alcohol intoxication |
Acute cyclitis |
Acute cyclitis |
Acute erosive gastritis |
Acute erosive gastritis (disorder) |
Acute exudative glomerulonephritis |
Acute exudative glomerulonephritis (disorder) |
Acute female pelvic cellulitis |
Acute female pelvic cellulitis |
Acute gastric erosion associated with severe burns |
Curling's ulcers |
Acute haemorrhagic gastritis |
Acute hemorrhagic gastritis |
Acute hemorrhagic gastritis |
Acute hemorrhagic gastritis |
Acute inflammatory demyelinating polyradiculoneuropathy |
A rare inflammatory neuropathy belonging to the clinical spectrum of Guillain-Barré syndrome (GBS). |
Acute iridocyclitis |
Acute iridocyclitis |
Acute mixed lineage leukaemia |
Mixed phenotype acute leukaemia |
Acute mixed lineage leukemia |
Mixed phenotype acute leukaemia |
Acute mucopurulent inflammation |
Acute mucopurulent discharge (morphologic abnormality) |
Acute myeloblastic leukaemia |
Acute myeloid leukemia with minimal differentiation |
Acute myeloblastic leukemia |
Acute myeloid leukemia with minimal differentiation |
Acute myelofibrosis |
A rare unclassified acute myeloid leukemia characterized by an acute panmyeloid proliferation with blasts constituting more than 20% of cells in the bone marrow or peripheral blood, accompanied by fibrosis of the bone marrow. Patients typically present with acute onset of severe constitutional symptoms, bone pain, and pancytopenia. Splenomegaly is minimal or absent. The disease is rapidly progressive with poor therapy response. |
Acute myeloid leukaemia |
Acute myeloid leukemia - category |
Acute myeloid leukaemia |
Acute myeloid leukemia (morphologic abnormality) |
Acute myeloid leukaemia with 11q23 abnormality |
A rare tumor arising from hematopoietic and lymphoid tissues characterized by abnormal proliferation and differentiation of a clonal population of myeloid stem cells carrying unspecific 11q23 abnormalities. Clinical manifestations result from accumulation of malignant myeloid cells within the bone marrow, peripheral blood and other organs, and include leukocytosis, anemia, thrombocytopenia, fatigue, anorexia and weight loss. |
Acute myeloid leukemia |
Acute myeloid leukemia (morphologic abnormality) |
Acute myeloid leukemia with 11q23 abnormality |
A rare tumor arising from hematopoietic and lymphoid tissues characterized by abnormal proliferation and differentiation of a clonal population of myeloid stem cells carrying unspecific 11q23 abnormalities. Clinical manifestations result from accumulation of malignant myeloid cells within the bone marrow, peripheral blood and other organs, and include leukocytosis, anemia, thrombocytopenia, fatigue, anorexia and weight loss. |
Acute myeloid leukemia with t(9;11)(p22;q23); MLLT3-MLL |
Acute myeloid leukemia with KMT2A rearrangement (morphologic abnormality) |
Acute peripheral vestibulopathy |
Vestibular neuronitis of inner ear (disorder) |
Acute renal failure |
Acute kidney injury (disorder) |
Acute rheumatic carditis |
Acute rheumatic carditis |
Acute tubular necrosis |
Acute tubular necrosis |
Acute vestibular neuronitis |
Vestibular neuronitis of inner ear (disorder) |
Acyl-ACP dehydrogenase |
Enoyl-[acyl-carrier protein] reductase (NADPH, A-specific) |
Addisonian crisis |
A primary adrenal insufficiency caused by a sudden defective production of adrenal steroids (cortisol and aldosterone). It represents an emergency, thus the rapid recognition and prompt therapy are critical for survival even before the diagnosis is made. |
Adenocarcinoma in situ in a polyp |
Adenocarcinoma in situ in a polyp |
Adenocarcinoma of accessory sinus |
Adenocarcinoma of accessory sinus |
Adenocarcinoma of ethmoidal sinus |
Adenocarcinoma of ethmoidal sinus (disorder) |