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
External Links
Disease Ontology
DOID:12801
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 1 - 10 of 44 in total
Gene ID Gene Symbol Description Source
175 AGA aspartylglucosaminidase
176 ACAN aggrecan
353 APRT adenine phosphoribosyltransferase
410 ARSA arylsulfatase A
411 ARSB arylsulfatase B
821 CANX calnexin
847 CAT catalase
912 CD1D CD1d molecule
952 CD38 CD38 molecule
1103 CHAT choline O-acetyltransferase
The Human Phenotype Ontology
Displaying entries 31 - 40 of 69 in total
HPO ID HPO Term
HP:0001260 Dysarthria
HP:0001263 Global developmental delay
HP:0001272 Cerebellar atrophy
HP:0001344 Absent speech
HP:0001348 Brisk reflexes
HP:0001385 Hip dysplasia
HP:0001387 Joint stiffness
HP:0001507 Growth abnormality
HP:0001653 Mitral regurgitation
HP:0001670 Asymmetric septal hypertrophy
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: August 19, 2024