Pub. Date : 2017 Sep
PMID : 28649514
2 Functional Relationships(s)Download |
Sentence | Compound Name | Protein Name | Organism |
1 | Mucopolysaccharidosis type II (MPS II - Hunter syndrome) is an X-linked lysosomal storage disorder caused by a deficiency in the enzyme iduronate-2 sulfatase (I2S), leading to the accumulation of the glycosaminoglycans, affecting multiple organs and systems. | Glycosaminoglycans | iduronate 2-sulfatase | Homo sapiens |
2 | Mucopolysaccharidosis type II (MPS II - Hunter syndrome) is an X-linked lysosomal storage disorder caused by a deficiency in the enzyme iduronate-2 sulfatase (I2S), leading to the accumulation of the glycosaminoglycans, affecting multiple organs and systems. | Glycosaminoglycans | iduronate 2-sulfatase | Homo sapiens |