mucopolysaccharidosis II

Summary
Synonym
  • Hunter syndrome
  • Hunter's syndrome
  • MPS II - Hunter syndrome
  • Mucopolysaccharidosis, MPS-II
  • deficiency of iduronate-2-sulphatase
Definition
A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase.
Super Class
mucopolysaccharidosis
Disease Ontology
DOID:12799
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3423 IDS iduronate 2-sulfatase
Displaying 1 entry
Gene ID Gene Symbol Description Source
15931 Ids iduronate 2-sulfatase
The Human Phenotype Ontology
Displaying entries 101 - 109 of 109 in total
HPO ID HPO Term
HP:0003510 Severe short stature
HP:0003541 Urinary glycosaminoglycan excretion
HP:0003593 Infantile onset
HP:0003621 Juvenile onset
HP:0004389 Intestinal pseudo-obstruction
HP:0006532 Recurrent pneumonia
HP:0006536 Airway obstruction
HP:0011462 Young adult onset
HP:0011463 Childhood onset
Displaying 1 entry
Gene ID Gene Symbol Description
3423 IDS iduronate 2-sulfatase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024