Terminology Service < Semantic Lookup Platform

All terms in MESHD

Label	Id	Description
Coronary Aneurysm	D003323	[Abnormal balloon- or sac-like dilatation in the wall of CORONARY VESSELS. Most coronary aneurysms are due to CORONARY ATHEROSCLEROSIS, and the rest are due to inflammatory diseases, such as KAWASAKI DISEASE.]
Empyema, Tuberculous	D004654	[Empyema due to MYCOBACTERIUM TUBERCULOSIS.]
Tuberculosis, Pleural	D014396	[Tuberculosis of the serous membrane lining the thoracic cavity and surrounding the lungs.]
Coronary Thrombosis	D003328	[Coagulation of blood in any of the CORONARY VESSELS. The presence of a blood clot (THROMBUS) often leads to MYOCARDIAL INFARCTION.]
Thrombosis	D013927	[Formation and development of a thrombus or blood clot in the blood vessel.]
Coronary Vasospasm	D003329	[Spasm of the large- or medium-sized coronary arteries.]
Critical Illness	D016638	[A disease or state in which death is possible or imminent.]
Olfactory Nerve Injuries	D061219	[Traumatic injuries to the OLFACTORY NERVE. It may result in various olfactory dysfunction including a complete loss of smell.]
Olfactory Nerve Diseases	D020431	[Diseases of the first cranial (olfactory) nerve, which usually feature anosmia or other alterations in the sense of smell and taste. Anosmia may be associated with NEOPLASMS; CENTRAL NERVOUS SYSTEM INFECTIONS; CRANIOCEREBRAL TRAUMA; inherited conditions; toxins; METABOLIC DISEASES; tobacco abuse; and other conditions. (Adams et al., Principles of Neurology, 6th ed, pp229-31)]
Cranial Nerve Injuries	D020209	[Dysfunction of one or more cranial nerves causally related to a traumatic injury. Penetrating and nonpenetrating CRANIOCEREBRAL TRAUMA; NECK INJURIES; and trauma to the facial region are conditions associated with cranial nerve injuries.]
Coronary Vessel Anomalies	D003330	[Malformations of CORONARY VESSELS, either arteries or veins. Included are anomalous origins of coronary arteries; ARTERIOVENOUS FISTULA; CORONARY ANEURYSM; MYOCARDIAL BRIDGING; and others.]
Coronaviridae Infections	D003333	[Virus diseases caused by CORONAVIRIDAE.]
Brucellosis	D002006	[Infection caused by bacteria of the genus BRUCELLA mainly involving the MONONUCLEAR PHAGOCYTE SYSTEM. This condition is characterized by fever, weakness, malaise, and weight loss., Human BRUCELLA infection with pulmonary involvement such as EMPYEMA; LUNG ABSCESS; and PLEURAL EFFUSION.]
Brucellosis, Bovine	D002007	[A disease of cattle caused by bacteria of the genus BRUCELLA leading to abortion in late pregnancy. BRUCELLA ABORTUS is the primary infective agent.]
Abortion, Veterinary	D000034	[Premature expulsion of the FETUS in animals.]
Rickettsia Infections	D012282	[Infections by the genus RICKETTSIA.]
Encephalopathy, Bovine Spongiform	D016643	[A transmissible spongiform encephalopathy of cattle associated with abnormal prion proteins in the brain. Affected animals develop excitability and salivation followed by ATAXIA. This disorder has been associated with consumption of SCRAPIE infected ruminant derived protein. This condition may be transmitted to humans, where it is referred to as variant or new variant CREUTZFELDT-JAKOB SYNDROME. (Vet Rec 1998 Jul 25;143(41):101-5)]
Primary Ovarian Insufficiency	D016649	[A form of ovarian failure, caused by resistance to GONADOTROPINS stimulation. It may be caused by defects in the receptors for FOLLICLE STIMULATING HORMONE or LUTEINIZING HORMONE. It may be due to factors interfering with the actions of gonadotropins, such as antibodies blocking the ligand-receptor interaction., Cessation of ovarian function after MENARCHE but before the age of 40, without or with OVARIAN FOLLICLE depletion. It is characterized by the presence of OLIGOMENORRHEA or AMENORRHEA, elevated GONADOTROPINS, and low ESTRADIOL levels. It is a state of female HYPERGONADOTROPIC HYPOGONADISM. Etiologies include genetic defects, autoimmune processes, chemotherapy, radiation, and infections. The most commonly known genetic cause is the expansion of a CGG repeat to 55 to 199 copies in the 5' untranslated region in the X-linked FMR1 gene.]
Ovarian Diseases	D010049	[Pathological processes of the OVARY.]
Fructose Metabolism, Inborn Errors	D015318	[Inherited abnormalities of fructose metabolism, which include three known autosomal recessive types: hepatic fructokinase deficiency (essential fructosuria), hereditary fructose intolerance, and hereditary fructose-1,6-diphosphatase deficiency. Essential fructosuria is a benign asymptomatic metabolic disorder caused by deficiency in fructokinase, leading to decreased conversion of fructose to fructose-1-phosphate and alimentary hyperfructosemia, but with no clinical dysfunction; may produce a false-positive diabetes test.]