Terminology Service < Semantic Lookup Platform

All individuals in MESHD

Label	Id	Description
Sheep Diseases	D012757	[Diseases of domestic and mountain sheep of the genus Ovis.]
Shellfish Hypersensitivity	D000067208	[Allergic reaction to SHELLFISH or shellfish products.]
Shellfish Poisoning	D057096	[A condition caused by ingestion of shellfish contaminated with SAXITOXIN from dinoflagellate species in the genus Alexandrium., A condition caused by ingestion of shellfish contaminated with brevetoxins primarily produced by the marine dinoflagellate Karenia brevis. This results from a HARMFUL ALGAL BLOOM, especially the so-called "Florida red tide.", Poisoning from toxins present in bivalve mollusks that have been ingested. Four distinct types of shellfish poisoning are recognized based on the toxin involved., A condition caused by ingestion of shellfish contaminated with toxins from Dinophysis species., A condition caused by ingestion of shellfish contaminated by domoic acid-producing diatoms of the genus Pseudo-nitzschia.]
Shock	D012769	[A pathological condition manifested by failure to perfuse or oxygenate vital organs.]
Shock, Cardiogenic	D012770	[Shock resulting from diminution of cardiac output in heart disease.]
Shock, Hemorrhagic	D012771	[Acute hemorrhage or excessive fluid loss resulting in HYPOVOLEMIA.]
Shock, Septic	D012772	[Sepsis associated with HYPOTENSION or hypoperfusion despite adequate fluid resuscitation. Perfusion abnormalities may include, but are not limited to LACTIC ACIDOSIS; OLIGURIA; or acute alteration in mental status.]
Shock, Surgical	D012773	[A type of shock that occurs as a result of a surgical procedure.]
Shock, Traumatic	D012774	[Shock produced as a result of trauma.]
Short Bowel Syndrome	D012778	[A malabsorption syndrome resulting from extensive operative resection of the SMALL INTESTINE, the absorptive region of the GASTROINTESTINAL TRACT.]
Short Rib-Polydactyly Syndrome	D012779	[A syndrome inherited as an autosomal recessive trait and incompatible with life. The main features are narrow thorax, short ribs, scapular and pelvic dysplasia, and polydactyly.]
Shoulder Dislocation	D012783	[Displacement of the HUMERUS from the SCAPULA.]
Shoulder Fractures	D012784	[Fractures of the proximal humerus, including the head, anatomic and surgical necks, and tuberosities.]
Shoulder Impingement Syndrome	D019534	[Compression of the ROTATOR CUFF tendons and subacromial bursa between the HUMERAL HEAD and the ACROMION of the SCAPULA. This condition is associated with subacromial BURSITIS, as well as rotator cuff (largely supraspinatus) and bicipital tendon INFLAMMATION.]
Shoulder Injuries	D000070599	[Injuries involving the SHOULDERS.]
Shoulder Pain	D020069	[Unilateral or bilateral pain of the shoulder. It is often caused by physical activities such as work or sports participation, but may also be pathologic in origin.]
Shwartzman Phenomenon	D012790	[Hemorrhagic necrosis that was first demonstrated in rabbits with a two-step reaction, an initial local (intradermal) or general (intravenous) injection of a priming endotoxin (ENDOTOXINS) followed by a second intravenous endotoxin injection (provoking agent) 24 h later. The acute inflammation damages the small blood vessels. The following intravascular coagulation leads to capillary and venous THROMBOSIS and NECROSIS. Shwartzman phenomenon can also occur in other species with a single injection of a provoking agent, and during infections or pregnancy. Its susceptibility depends on the status of IMMUNE SYSTEM, coagulation, FIBRINOLYSIS, and blood flow.]
Shy-Drager Syndrome	D012791	[A progressive neurodegenerative condition of the central and autonomic nervous systems characterized by atrophy of the preganglionic lateral horn neurons of the thoracic spinal cord. This disease is generally considered a clinical variant of MULTIPLE SYSTEM ATROPHY. Affected individuals present in the fifth or sixth decade with ORTHOSTASIS and bladder dysfunction; and later develop FECAL INCONTINENCE; anhidrosis; ATAXIA; IMPOTENCE; and alterations of tone suggestive of basal ganglia dysfunction. (From Adams et al., Principles of Neurology, 6th ed, p536)]
Sialadenitis	D012793	[INFLAMMATION of salivary tissue (SALIVARY GLANDS), usually due to INFECTION or injuries.]
Sialic Acid Storage Disease	D029461	[Autosomal recessive neurodegenerative disorders caused by lysosomal membrane transport defects that result in accumulation of free sialic acid (N-ACETYLNEURAMINIC ACID) within the lysosomes. The two main clinical phenotypes, which are allelic variants of the SLC17A5 gene, are ISSD, a severe infantile form, or Salla disease, a slowly progressive adult form, named for the geographic area in Finland where the kindred first studied resided.]