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bn:03372356n
Noun Concept
Categories: Proteoglycan metabolism disorders, Articles with permanently dead external links, Rare syndromes, Diseases named for discoverer, Syndromes
EN
Hunter syndrome  mucopolysaccharidosis II  Mucopolysaccharidosis, MPS-II  deficiency of iduronate-2-sulphatase  Hunter's disease
EN
Hunter syndrome, or mucopolysaccharidosis type II, is a rare genetic disorder in which large sugar molecules called glycosaminoglycans build up in body tissues. Wikipedia
English:
hunter
Definitions
Relations
Sources
EN
Hunter syndrome, or mucopolysaccharidosis type II, is a rare genetic disorder in which large sugar molecules called glycosaminoglycans build up in body tissues. Wikipedia
A hereditary disease Wikipedia Disambiguation
Mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase Wikidata
IS A
rare disease
hypertrophic cardiomyopathy
mucopolysaccharidosis
ptosis
DRUG USED FOR TREATMENT
idursulfase
GENETIC ASSOCIATION
iduronate-2-sulfatase
HEALTH SPECIALTY
endocrinology
MODE OF INHERITANCE
X-linked recessive inheritance
Wikipedia
EN
Hunter syndrome
Wikidata
EN
mucopolysaccharidosis II
Wikipedia Redirections
EN
Hunter's disease, Hunter's syndrome, Hunter's Syndrome, Hunter Syndrome, Hunter syndrome (MPS II), Iduronate 2-sulfatase deficiency, Mucopolysaccharidosis, type II, Mucopolysaccharidosis ii, Mucopolysaccharidosis II, Mucopolysaccharidosis type 2 Hunter syndrome- mild form, Mucopolysaccharidosis type 2 Hunter syndrome- severe form
Wikidata Alias
EN
deficiency of iduronate-2-sulphatase, Hunter's syndrome, Hunter syndrome, Ids Deficiency, Iduronate 2-Sulfatase Deficiency, MPS2, Mps 2, MPS II, MPS II - Hunter syndrome, MPSII, Mucopolysaccharidosis, MPS-II, MUCOPOLYSACCHARIDOSIS, TYPE II, MUCOPOLYSACCHARIDOSIS, TYPE II; MPS2, mucopolysaccharidosis II, mucopolysaccharidosis type 2, mucopolysaccharidosis type II, Sids Deficiency, Sulfoiduronate Sulfatase Deficiency

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