mucopolysaccharidosis III

Summary
Synonym
  • Mucopolysaccharidosis, MPS-III
  • N-sulphoglucosamine sulphohydrolase deficiency
  • Sanfilippo's syndrome
  • heparan sulfate sulfatase deficiency
Definition
A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme resulting in incomplete breakdown of the heparan sulfate sugar chain.
Super Class
mucopolysaccharidosis
Disease Ontology
DOID:12801
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
2799 GNS glucosamine (N-acetyl)-6-sulfatase
4669 NAGLU N-acetyl-alpha-glucosaminidase
6448 SGSH N-sulfoglucosamine sulfohydrolase
138050 HGSNAT heparan-alpha-glucosaminide N-acetyltransferase
Displaying all 4 entries
Gene ID Gene Symbol Description Source
27029 Sgsh N-sulfoglucosamine sulfohydrolase (sulfamidase)
27419 Naglu alpha-N-acetylglucosaminidase (Sanfilippo disease IIIB)
52120 Hgsnat heparan-alpha-glucosaminide N-acetyltransferase
75612 Gns glucosamine (N-acetyl)-6-sulfatase
Displaying 1 entry
Gene ID Gene Symbol Description Source
175063 K09E4.4 Alpha-N-acetylglucosaminidase
The Human Phenotype Ontology
Displaying entries 11 - 20 of 69 in total
HPO ID HPO Term
HP:0000369 Low-set ears
HP:0000403 Recurrent otitis media
HP:0000463 Anteverted nares
HP:0000470 Short neck
HP:0000490 Deeply set eye
HP:0000505 Visual impairment
HP:0000574 Thick eyebrow
HP:0000662 Nyctalopia
HP:0000664 Synophrys
HP:0000711 Restlessness
Displaying 1 entry
Gene ID Gene Symbol Description
2799 GNS glucosamine (N-acetyl)-6-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