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bn:01012746n
Noun Concept
Categories: Rare diseases, Autosomal recessive disorders, Glycoprotein metabolism disorders
EN
galactosialidosis  Cathepsin a Deficiency  Cathepsin A deficiency of  GALACTOSIALIDOSIS; GSL  Goldberg Syndrome
EN
Galactosialidosis, also known as Neuraminidase deficiency with beta-galactosidase deficiency, is a genetic lysosomal storage disease. Wikipedia
Definitions
Relations
Sources
EN
Galactosialidosis, also known as Neuraminidase deficiency with beta-galactosidase deficiency, is a genetic lysosomal storage disease. Wikipedia
Rare disease Wikidata
IS A
rare disease
lysosomal storage disease
neurometabolic disease
GENETIC ASSOCIATION
Cathepsin A
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
galactosialidosis
Wikidata
EN
galactosialidosis
Wikipedia Redirections
EN
Neuraminidase beta-galactosidase deficiency
Wikidata Alias
EN
Cathepsin a Deficiency, Cathepsin A deficiency of, GALACTOSIALIDOSIS, GALACTOSIALIDOSIS; GSL, Goldberg Syndrome, GSL, Lysosomal Protective Protein Deficiency, Lysosomal protective protein deficiency of, Neuraminidase/Beta-Galactosidase Expression, Neuraminidase Deficiency With Beta-Galactosidase Deficiency, Ppca Deficiency, Protective Protein/Cathepsin a Deficiency

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