Pub. Date : 2022 Apr 27
PMID : 35563245
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Mucopolysaccharidosis type II (Hunter Syndrome) is a rare, x-linked recessive, progressive, multi-system, lysosomal storage disease caused by the deficiency of iduronate-2-sulfatase (IDS), which leads to the pathological storage of glycosaminoglycans in nearly all cell types, tissues and organs. | Glycosaminoglycans | iduronate 2-sulfatase | Homo sapiens |
2 | Mucopolysaccharidosis type II (Hunter Syndrome) is a rare, x-linked recessive, progressive, multi-system, lysosomal storage disease caused by the deficiency of iduronate-2-sulfatase (IDS), which leads to the pathological storage of glycosaminoglycans in nearly all cell types, tissues and organs. | Glycosaminoglycans | iduronate 2-sulfatase | Homo sapiens |