Fabry disease

Summary
Synonym
  • Alpha-galactosidase A deficiency
  • Angiokeratoma Corporis Diffusum
  • Fabry Disease, Cardiac Variant
  • Fabry's disease
  • alpha galactosidase deficiency
  • deficiency of melibiase
Definition
A sphingolipidosis that is characterized by the buildup of globotriaosylceramide in the body's cells and has_material_basis_in X-linked inherited mutations in the GLA gene, encoding alpha-galactosidase A, on chromosome Xq22.
Super Class
sphingolipidosis
External Links
Disease Ontology
DOID:14499
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 11 - 20 of 45 in total
Gene ID Gene Symbol Description Source
2581 GALC galactosylceramidase
2629 GBA1 glucosylceramidase beta 1
2632 GBE1 1,4-alpha-glucan branching enzyme 1
2717 GLA galactosidase alpha
2720 GLB1 galactosidase beta 1
2990 GUSB glucuronidase beta
3383 ICAM1 intercellular adhesion molecule 1
3423 IDS iduronate 2-sulfatase
3425 IDUA alpha-L-iduronidase
3958 LGALS3 galectin 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
17939 Naga N-acetyl galactosaminidase, alpha
Displaying 1 entry
Gene ID Gene Symbol Description Source
315165 Naga alpha-N-acetylgalactosaminidase
The Human Phenotype Ontology
Displaying entries 51 - 60 of 80 in total
HPO ID HPO Term
HP:0003077 Hyperlipidemia
HP:0003119 Abnormal circulating lipid concentration
HP:0003326 Myalgia
HP:0004306 Abnormal endocardium morphology
HP:0004322 Short stature
HP:0004349 Reduced bone mineral density
HP:0006510 Chronic pulmonary obstruction
HP:0007957 Corneal opacity
HP:0011675 Arrhythmia
HP:0011710 Bundle branch block
Displaying 1 entry
Gene ID Gene Symbol Description
2717 GLA galactosidase alpha

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