Terminology Service < Semantic Lookup Platform

All individuals in MESHD

Label	Id	Description
Wounds, Gunshot	D014948	[Disruption of structural continuity of the body as a result of the discharge of firearms.]
Wounds, Nonpenetrating	D014949	[Injuries caused by impact with a blunt object where there is no penetration of the skin.]
Wounds, Penetrating	D014950	[Wounds caused by objects penetrating the skin.]
Wounds, Stab	D014951	[Penetrating wounds caused by a pointed object.]
Wrist Injuries	D014954	[Injuries to the wrist or the wrist joint.]
X-Linked Combined Immunodeficiency Diseases	D053632	[Forms of combined immunodeficiency caused by mutations in the gene for INTERLEUKIN RECEPTOR COMMON GAMMA SUBUNIT. Both severe and non-severe subtypes of the disease have been identified.]
XYY Karyotype	D014997	[Abnormal genetic constitution in males characterized by an extra Y chromosome.]
Xanthogranuloma, Juvenile	D014972	[Benign disorder of infants and children caused by proliferation of HISTIOCYTES, macrophages found in tissues. These histiocytes, usually lipid-laden non-Langerhans cells, form multiple yellow-red nodules most often in the skin, the eye, and sometimes in the viscera. Patients appear to have normal lipid metabolism and are classified as a normolipemic non-Langerhans cell histiocytosis.]
Xanthomatosis	D014973	[A condition marked by the development of widespread xanthomas, yellow tumor-like structures filled with lipid deposits. Xanthomas can be found in a variety of tissues including the SKIN; TENDONS; joints of KNEES and ELBOWS. Xanthomatosis is associated with disturbance of LIPID METABOLISM and formation of FOAM CELLS.]
Xanthomatosis, Cerebrotendinous	D019294	[An autosomal recessive lipid storage disorder due to mutation of the gene CYP27A1 encoding a CHOLESTANETRIOL 26-MONOOXYGENASE. It is characterized by large deposits of CHOLESTEROL and CHOLESTANOL in various tissues resulting in xanthomatous swelling of tendons, early CATARACT, and progressive neurological symptoms.]
Xeroderma Pigmentosum	D014983	[A rare, pigmentary, and atrophic autosomal recessive disease. It is manifested as an extreme photosensitivity to ULTRAVIOLET RAYS as the result of a deficiency in the enzyme that permits excisional repair of ultraviolet-damaged DNA.]
Xerophthalmia	D014985	[Dryness of the eye surfaces caused by deficiency of tears or conjunctival secretions. It may be associated with vitamin A deficiency, trauma, or any condition in which the eyelids do not close completely.]
Xerostomia	D014987	[Decreased salivary flow.]
Yang Deficiency	D016711	[In the YIN-YANG system of philosophy and medicine, a lack of vital energy (called yangxu in Chinese). It manifests itself in various systemic and organic diseases. (The Pinyin Chinese-English Dictionary, 1979)]
Yaws	D015001	[A systemic non-venereal infection of the tropics caused by TREPONEMA PALLIDUM subspecies pertenue.]
Yellow Fever	D015004	[An acute infectious disease primarily of the tropics, caused by a virus and transmitted to man by mosquitoes of the genera Aedes and Haemagogus. The severe form is characterized by fever, HEMOLYTIC JAUNDICE, and renal damage.]
Yellow Nail Syndrome	D056684	[A rare condition characterized by the presence of yellow nails, LYMPHEDEMA, and/or PLEURAL EFFUSION with respiratory tract involvement. Abnormal lymphatic network may play a role in its etiology. Occasionally inherited, yellow nail syndrome mostly is sporadic without apparent family history.]
Yersinia Infections	D015009	[Infections with bacteria of the genus YERSINIA.]
Yersinia pseudotuberculosis Infections	D015012	[Infections with bacteria of the species YERSINIA PSEUDOTUBERCULOSIS.]
Yin Deficiency	D016710	[In the YIN-YANG system of philosophy and medicine, an insufficiency of body fluid (called yinxu), manifesting often as irritability, thirst, constipation, etc. (The Pinyin Chinese-English Dictionary, 1979).]