Terminology Service < Semantic Lookup Platform

All individuals in MESHD

Label	Id	Description
Vulvovaginitis	D014848	[Inflammation of the VULVA and the VAGINA, characterized by discharge, burning, and PRURITUS.]
WAGR Syndrome	D017624	[A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of WILMS TUMOR; ANIRIDIA; GENITOURINARY ABNORMALITIES; and INTELLECTUAL DISABILITY.]
Waardenburg Syndrome	D014849	[Rare, autosomal dominant disease with variable penetrance and several known clinical types. Characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and especially dystopia canthorum. The underlying cause may be defective development of the neural crest (neurocristopathy). Waardenburg's syndrome may be closely related to piebaldism. Klein-Waardenburg Syndrome refers to a disorder that also includes upper limb abnormalities.]
Waldenstrom Macroglobulinemia	D008258	[A lymphoproliferative disorder characterized by pleomorphic B-LYMPHOCYTES including PLASMA CELLS, with increased levels of monoclonal serum IMMUNOGLOBULIN M. There is lymphoplasmacytic cells infiltration into bone marrow and often other tissues, also known as lymphoplasmacytic lymphoma. Clinical features include ANEMIA; HEMORRHAGES; and hyperviscosity.]
Walker-Warburg Syndrome	D058494	[Rare autosomal recessive lissencephaly type 2 associated with congenital MUSCULAR DYSTROPHY and eye anomalies (e.g., RETINAL DETACHMENT; CATARACT; MICROPHTHALMOS). It is often associated with additional brain malformations such as HYDROCEPHALY and cerebellar hypoplasia and is the most severe form of the group of related syndromes (alpha-dystroglycanopathies) with common congenital abnormalities in the brain, eye and muscle development.]
Wallerian Degeneration	D014855	[Degeneration of distal aspects of a nerve axon following injury to the cell body or proximal portion of the axon. The process is characterized by fragmentation of the axon and its MYELIN SHEATH.]
Wandering Spleen	D050805	[A congenital or acquired condition in which the SPLEEN is not in its normal anatomical position but moves about in the ABDOMEN. This is due to laxity or absence of suspensory ligaments which normally provide peritoneal attachments to keep the SPLEEN in a fixed position. Clinical symptoms include ABDOMINAL PAIN, splenic torsion and ISCHEMIA.]
War-Related Injuries	D000067398	[Distress resulting from severe injuries., WOUNDS and INJURIES and PSYCHOLOGICAL TRAUMA sustained during WAR.]
Warts	D014860	[Benign epidermal proliferations or tumors; some are viral in origin.]
Wasting Disease, Chronic	D034081	[A transmissible spongiform encephalopathy (prion disease) of DEER and elk characterized by chronic weight loss leading to death. It is thought to spread by direct contact between animals or through environmental contamination with the prion protein (PRIONS).]
Wasting Syndrome	D019282	[A condition of involuntary weight loss of greater then 10% of baseline body weight. It is characterized by atrophy of muscles and depletion of lean body mass. Wasting is a sign of MALNUTRITION as a result of inadequate dietary intake, malabsorption, or hypermetabolism.]
Water Intoxication	D014869	[A condition resulting from the excessive retention of water with sodium depletion.]
Water-Electrolyte Imbalance	D014883	[Disturbances in the body's WATER-ELECTROLYTE BALANCE.]
Waterborne Diseases	D000069578	[Illnesses due to micro-organisms and chemicals in drinking water, those caused by organisms having part of their lifecycle in water or those with water-related vectors, and others spread by aerosols containing pathogens.]
Waterhouse-Friderichsen Syndrome	D014884	[A condition of HEMORRHAGE and NECROSIS of the ADRENAL GLAND. It is characterized by rapidly developing ADRENAL INSUFFICIENCY; HYPOTENSION; and widespread cutaneous PURPURA.]
Weight Gain	D015430	[Increase in BODY WEIGHT over existing weight.]
Weight Loss	D015431	[Decrease in existing BODY WEIGHT.]
Weil Disease	D014895	[A severe form of LEPTOSPIROSIS, usually caused by LEPTOSPIRA INTERROGANS SEROVAR ICTEROHAEMORRHAGIAE and occasionally other serovars. It is transmitted to humans by the rat and is characterized by hemorrhagic and renal symptoms with accompanying JAUNDICE.]
Weill-Marchesani Syndrome	D056846	[The autosomal dominant form of Weill-Marchesani syndrome is associated with Adamts10 gene mutations., The autosomal recessive form of Weill-Marchesani syndrome is associated with Fibrillin gene mutations., Rare congenital disorder of connective tissue characterized by brachydactyly, joint stiffness, childhood onset of ocular abnormalities (e.g., microspherophakia, ECTOPIA LENTIS; GLAUCOMA), and proportionate short stature. Cardiovascular anomalies are occasionally seen.]
Werner Syndrome	D014898	[An autosomal recessive disorder that causes premature aging in adults, characterized by sclerodermal skin changes, cataracts, subcutaneous calcification, muscular atrophy, a tendency to diabetes mellitus, aged appearance of the face, baldness, and a high incidence of neoplastic disease.]