Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 CausalMutation disease CLINVAR How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports. 28858097 2017
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease CLINVAR Advantages of early replacement therapy for mucopolysaccharidosis type VI: echocardiographic follow-up of siblings. 23458163 2014
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 CausalMutation disease CLINVAR A long term follow-up study of the development of hip disease in Mucopolysaccharidosis type VI. 28552677 2017
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease BEFREE Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome), a rare autosomal recessive lysosomal storage disease, is caused by mutations in the N-acetylgalactosamine-4-sulfatase (arylsulfatase B, or ARSB) gene, resulting in a deficiency of ARSB activity. 27797586 2017
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 CausalMutation disease CLINVAR Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome) is a lysosomal storage disorder caused by mutations in the N-acetylgalactosamine-4-sulfatase (arylsulfatase B, ARSB) gene. 17458871 2007
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 Biomarker disease BEFREE Mucopolysaccharidosis type VI (MPS VI) or Maroteaux-Lamy syndrome is produced by the deficiency of the enzyme arylsulfatase B, responsible for the hydrolysis of N-acetyl-D-galactosamine, chondroitin sulfate, and dermatan sulfate. 30335002 2018
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease CLINVAR Maroteaux-Lamy syndrome is an autosomal-recessive disorder due to the deficit of the lysosomal enzyme, arylsulfatase B (ARSB). 19259130 2009
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 CausalMutation disease CLINVAR Clinical manifestations of 17 patients affected with mucopolysaccharidosis type VI and eight novel ARSB mutations. 24677745 2014
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 Biomarker disease BEFREE Direct comparison of measures of endurance, mobility, and joint function during enzyme-replacement therapy of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): results after 48 weeks in a phase 2 open-label clinical study of recombinant human N-acetylgalactosamine 4-sulfatase. 15930196 2005
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease BEFREE Identification of eleven different mutations including six novel, in the arylsulfatase B gene in Iranian patients with mucopolysaccharidosis type VI. 30982216 2019
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 CausalMutation disease CLINVAR Four novel mutant alleles of the arylsulfatase B gene in two patients with intermediate form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). 8125475 1994
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease BEFREE Large deletion involving exon 5 of the arylsulfatase B gene caused apparent homozygosity in a mucopolysaccharidosis type VI patient. 20143913 2010
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 Biomarker disease BEFREE Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome, MPS VI) is an autosomal recessive disorder caused by deficiency of N-acetylgalactosamine-4-sulphatase (ARSB),which leads to the lysosomal accumulation and excretion of dermatan sulphate (DS). 16435196 2005
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 CausalMutation disease CLINVAR Attenuated osteoarticular phenotype of type VI mucopolysaccharidosis: a report of four patients and a review of the literature. 24221504 2014
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease LHGDN Mucopolysaccharidosis type VI (MPS VI; Maroteaux-Lamy syndrome) is a lysosomal storage disorder caused by mutations in the N-acetylgalactosamine-4-sulfatase (arylsulfatase B, ARSB) gene. 17458871 2007
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 CausalMutation disease CLINVAR Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome): six unique arylsulfatase B gene alleles causing variable disease phenotypes. 8116615 1994
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease UNIPROT Four novel mutant alleles of the arylsulfatase B gene in two patients with intermediate form of mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). 8125475 1994
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease BEFREE Mucopolysaccharidosis VI (Maroteaux-Lamy syndrome). An intermediate clinical phenotype caused by substitution of valine for glycine at position 137 of arylsulfatase B. 1718978 1991
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease CLINVAR Molecular analysis of mucopolysaccharidosis type VI in Poland, Belarus, Lithuania and Estonia. 22133300 2012
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 Biomarker disease BEFREE Mucopolysaccharidosis type VI (MPS VI - Maroteaux-Lamy syndrome) is a globally rare lysosomal storage disease caused by a deficiency of arylsulfatase B. 25060283 2014
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease CLINVAR Novel mutations of the arylsulphatase B (ARSB) gene in Indian patients with mucopolysaccharidosis type VI. 26609033 2015
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 Biomarker disease BEFREE These data indicate that repeated IT-INJ of rhASB can safely prevent GAG storage in MPS-VI dura. 22289849 2012
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease BEFREE A 13-year-old child was clinically diagnosed with mucopolysaccharidosis type VI-Maroteaux-Lamy syndrome (MPS VI) at the age of 5 years, and the diagnosis was confirmed biochemically and genetically (homozygous mutation in ARSB gene). 27512882 2016
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 Biomarker disease RGD The ARSB gene was assigned to rat chromosome 2, where the locus for the MPS VI phenotype in rats has been localized by linkage analysis. 8575749 1995
Entrez Id: 411
Gene Symbol: ARSB
ARSB
1.000 GeneticVariation disease CLINVAR Prevalence of anti-adeno-associated virus serotype 8 neutralizing antibodies and arylsulfatase B cross-reactive immunologic material in mucopolysaccharidosis VI patient candidates for a gene therapy trial. 25654180 2015