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type II mucopolysaccharidosis - translation to English
MUCOPOLYSACCHARIDOSIS CHARACTERIZED BY A DEFICIENCY OF THE LYSOSOMAL ENZYME BETA-GLUCURONIDASE RESULTING IN THE INABILITY TO DEGRADE GLUCURONIC ACID-CONTAINING GLYCOSAMINOGLYCANS
Mucopolysaccharidosis type VII Sly syndrome; Mucopolysaccharidosis type VII; Mucopolysaccharidosis Type VII; Mucopolysaccharidosis VII; Mucopolysaccharidosis vii; Sly Syndrome; MPS VII
type II mucopolysaccharidosis
медицина
мукополисахаридоз II типа
синдром Гунтера
синдром Хантера
mucopolysaccharidosis
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.jpg?width=200 "Corneal clouding in a 30-year-old male with MPS-VI. Several other MPS disorders may also present with corneal clouding.")
LYSOSOMAL STORAGE DISEASE THAT INVOLVES THE ACCUMULATION OF GLYCOSAMINOGLYCANS IN THE TISSUES AND THEIR EXCRETION IN THE URINE
Mucopolysaccharidoses; Mucopolysaccharide disease; Mucopolysaccharoidosis; Mucopolysaccharidosis type 3; Mucopolysaccharidosis type 4; Mucopolysaccharidosis type I Hurler syndrome; Mucopolysaccharidosis type I Hurler/Scheie syndrome; Mucopolysaccharidosis type I Scheie syndrome; Mucopolysaccharidosis type II Hunter syndrome- mild form; Mucopolysaccharidosis type II Hunter syndrome- severe form; Mucopolysaccharidosis type IV-A Morquio syndrome; Mucopolysaccharidosis type IV-B; Mucopolysaccharidosis type V; Scheie's syndrome; Scheie's Syndrome; Mucopolysaccharidosis affecting the skin; Mucopolysaccharidosis I S (Scheie)
медицина
мукополисахаридоз
Langer-Saldino achondrogenesis
ACHONDROGENESIS THAT HAS MATERIAL BASIS IN MUTATIONS IN THE COL2A1 GENE WHICH RESULTS IN UNDERDEVELOPED LUNGS, HYDROPS FETALIS, A PROMINENT FOREHEAD AND ABNORMAL OSSIFICATION OF THE LOCATED IN VERTEBRAL COLUMN OR LOCATED IN PELVIS
Achondrogenesis type II; Langer-Saldino achondrogenesis; Achondrogenesis, type 2; Achondrogenesis-hypochondrogenesis type 2
медицина
ахондрогенез типа Лангера-Салдино
Definition
Мошеш II
Мшешве II (Moshesh, Moshweshwe) (р. 2.5.1938), король (главный вождь) Лесото с 1960. Старший сын главного вождя Симеона Сеисо Гриффита. Учился в Оксфорде. В декабре 1970 по требованию премьер-министра Л. Джонатана М. II принёс присягу, обязывающую его под угрозой низложения воздерживаться от всякой политической деятельности.
Wikipedia
Sly syndrome
Sly syndrome, also called mucopolysaccharidosis type VII (MPS-VII), is an autosomal recessive lysosomal storage disease caused by a deficiency of the enzyme β-glucuronidase. This enzyme is responsible for breaking down large sugar molecules called glycosaminoglycans (AKA GAGs, or mucopolysaccharides). The inability to break down GAGs leads to a buildup in many tissues and organs of the body. The severity of the disease can vary widely.
