NGLY1 deficiency [Supplementary Concept]

Date introduced: February 2, 2018

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Do not include MeSH terms found below this term in the MeSH hierarchy.

MeSH Unique ID: C000626124

Heading Mapped to:

• Congenital Disorders of Glycosylation
• Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase/deficiency

Entry Terms:

• Alacrimia-choreoathetosis-liver dysfunction syndrome
• Congenital disorder of deglycosylation
• Congenital disorder of glycosylation, type Iv

All MeSH Categories
NGLY1 deficiency