Terminology Service < Semantic Lookup Platform

All terms in MESHD

Label	Id	Description
Disease Resistance	D060467	[The capacity of an organism to defend itself against pathological processes or the agents of those processes. This most often involves innate immunity whereby the organism responds to pathogens in a generic way. The term disease resistance is used most frequently when referring to plants.]
Hypervitaminosis A	D006986	[A symptom complex resulting from ingesting excessive amounts of VITAMIN A.]
Hypesthesia	D006987	[Absent or reduced sensitivity to cutaneous stimulation.]
Collection	Collection	[A meaningful collection of concepts.]
Trisomy 13 Syndrome	D000073839	[A chromosome disorder associated with TRISOMY of all or part of CHROMOSOME 13. Clinical manifestations include CONGENITAL HEART DEFECTS (e.g., PATENT DUCTUS ARTERIOSUS), facial malformations (e.g., CLEFT LIP; CLEFT PALATE; COLOBOMA; MICROPHTHALMIA); HYPOTONIA, digit malformations (e.g., POLYDACTYLY or SYNDACTYLY), and SEIZURES and severe INTELLECTUAL DISABILITY associated with NERVOUS SYSTEM MALFORMATIONS.]
Hyphema	D006988	[Bleeding in the anterior chamber of the eye.]
Stomach Volvulus	D013277	[Twisting of the STOMACH that may result in gastric ISCHEMIA and GASTRIC OUTLET OBSTRUCTION. It is often associated with DIAPHRAGMATIC HERNIA.]
Stomach Ulcer	D013276	[Ulceration of the GASTRIC MUCOSA due to contact with GASTRIC JUICE. It is often associated with HELICOBACTER PYLORI infection or consumption of nonsteroidal anti-inflammatory drugs (NSAIDS).]
Stomach Rupture	D013275	[Bursting of the STOMACH.]
Stomach Neoplasms	D013274	[Tumors or cancer of the STOMACH.]
Diverticulum, Stomach	D013273	[Saccular, outward protrusion of all or a portion of the wall of the STOMACH.]
Stomatitis, Denture	D013282	[Inflammation of the mouth due to denture irritation.]
Stomatitis, Aphthous	D013281	[A recurrent disease of the oral mucosa of unknown etiology. It is characterized by small white ulcerative lesions, single or multiple, round or oval. Two to eight crops of lesions occur per year, lasting for 7 to 14 days and then heal without scarring. (From Jablonski's Dictionary of Dentistry, 1992, p742)]
Alveolar Bone Loss	D016301	[Resorption or wasting of the tooth-supporting bone (ALVEOLAR PROCESS) in the MAXILLA or MANDIBLE.]
Abnormalities, Radiation-Induced	D000016	[Congenital changes in the morphology of organs produced by exposure to ionizing or non-ionizing radiation.]
Hemospermia	D051516	[Blood in the SEMEN, usually due to INFLAMMATION of the PROSTATE, the SEMINAL VESICLES, or both.]
Abnormalities, Drug-Induced	D000014	[Congenital abnormalities caused by medicinal substances or drugs of abuse given to or taken by the mother, or to which she is inadvertently exposed during the manufacture of such substances. The concept excludes abnormalities resulting from exposure to non-medicinal chemicals in the environment.]
Abetalipoproteinemia	D000012	[An autosomal recessive disorder of lipid metabolism. It is caused by mutation of the microsomal triglyceride transfer protein that catalyzes the transport of lipids (TRIGLYCERIDES; CHOLESTEROL ESTERS; PHOSPHOLIPIDS) and is required in the secretion of BETA-LIPOPROTEINS (low density lipoproteins or LDL). Features include defective intestinal lipid absorption, very low serum cholesterol level, and near absent LDL.]
Hypoaldosteronism	D006994	[A selective aldosterone deficiency resulting from diminished RENIN-generated ANGIOTENSIN II, a key stimulus to aldosterone secretion. Previously, it was called type IV renal tubular acidosis., A congenital or acquired condition of insufficient production of ALDOSTERONE by the ADRENAL CORTEX leading to diminished aldosterone-mediated synthesis of Na(+)-K(+)-EXCHANGING ATPASE in renal tubular cells. Clinical symptoms include HYPERKALEMIA, sodium-wasting, HYPOTENSION, and sometimes metabolic ACIDOSIS.]
Funnel Chest	D005660	[A developmental anomaly in which the lower sternum is posteriorly dislocated and concavely deformed, resulting in a funnel-shaped thorax.]