mucopolysaccharidosis VI

Summary
Synonym
  • MPS VI - Maroteaux-Lamy syndrome
  • Maroteaux - Lamy syndrome
  • Maroteaux-Lamy syndrome
  • arylsulfatase B deficiency
  • deficiency of N-acetylgalactosamine-4-sulfatase
Definition
A mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme N-acetylgalactosamine 4-sulfatase.
Super Class
mucopolysaccharidosis
External Links
Disease Ontology
DOID:12800
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 21 - 30 of 41 in total
Gene ID Gene Symbol Description Source
3423 IDS iduronate 2-sulfatase
3425 IDUA alpha-L-iduronidase
3897 L1CAM L1 cell adhesion molecule
4125 MAN2B1 mannosidase alpha class 2B member 1
4669 NAGLU N-acetyl-alpha-glucosaminidase
4758 NEU1 neuraminidase 1
4907 NT5E 5'-nucleotidase ecto
5476 CTSA cathepsin A
6448 SGSH N-sulfoglucosamine sulfohydrolase
6677 SPAM1 sperm adhesion molecule 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
21926 Tnf tumor necrosis factor
Displaying 1 entry
Gene ID Gene Symbol Description Source
24835 Tnf tumor necrosis factor
The Human Phenotype Ontology
Displaying entries 41 - 50 of 63 in total
HPO ID HPO Term
HP:0002938 Lumbar hyperlordosis
HP:0003016 Metaphyseal widening
HP:0003025 Metaphyseal irregularity
HP:0003274 Hypoplastic acetabulae
HP:0003300 Ovoid vertebral bodies
HP:0003311 Hypoplasia of the odontoid process
HP:0003521 Disproportionate short-trunk short stature
HP:0003593 Infantile onset
HP:0004322 Short stature
HP:0005180 Tricuspid regurgitation
Displaying 1 entry
Gene ID Gene Symbol Description
411 ARSB arylsulfatase B

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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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