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Schindler Disease, Type I [Supplementary Concept]

Date introduced: August 25, 2010

MeSH Unique ID: C536631

Heading Mapped to:

Entry Terms:

  • Alpha-Naga Deficiency
  • Angiokeratoma Corporis Diffusum-Glycopeptiduria
  • Galb Deficiency
  • Lysosomal Glycoaminoacid Storage Disease-Angiokeratoma Corporis Diffusum
  • Naga Deficiency
  • Naga Deficiency, Type I
  • Neuroaxonal dystrophy, Schindler type
  • Neuronal Axonal Dystrophy, Schindler Type
  • Schindler Disease
  • Schindler disease, type 1
  • Alpha-Galactosidase B Deficiency
  • Alpha-Galnac Deficiency, Schindler Type
  • Alpha-N-Acetylgalactosaminidase Deficiency
  • Alpha-N-Acetylgalactosaminidase Deficiency, Type I
  • Alpha-N-acetylgalactosaminidase deficiency, type 1
  • Schindler Disease, Type II
  • Kanzaki disease
  • Alpha-N-acetylgalactosaminidase deficiency adult onset
  • Alpha-N-acetylgalactosaminidase deficiency type 2
  • Alpha-N-Acetylgalactosaminidase Deficiency, Adult-Onset
  • NAGA deficiency type 2
  • NAGA Deficiency, Type II
  • Schindler disease, type 2
  • alpha-N-Acetylgalactosaminidase Deficiency, Type II
  • Schindler Disease, Type III
  • Alpha-N-Acetylgalactosaminidase Deficiency, Type III
  • NAGA Deficiency, Type III

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