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Template:Glycoprotein disorders: Difference between revisions

From WikiMD's Medical Encyclopedia

Newer edit →
Revision as of 21:15, 13 August 2020 edit
en>Was a bee
m →top: ICD code exported (from bot request)
 
Revision as of 07:55, 30 April 2024 edit undo
Prab (talk | contribs)
, Bureaucrats, Interface administrators, Administrators
1,432,301 edits
CSV import
Newer edit →
Line 35: Line 35:
[[Category:Metabolic disorder templates]]
[[Category:Metabolic disorder templates]]
</noinclude>
</noinclude>
{{no-index-template}}

Revision as of 07:55, 30 April 2024

Lysosomal storage diseases: Inborn errors of carbohydrate metabolism (Glycoproteinoses)
Anabolism
* Dolichol kinase deficiency
  • Congenital disorder of glycosylation
Post-translational modification
of lysosomal enzymes
* Mucolipidosis: I-cell disease (ML II)
  • Pseudo-Hurler polydystrophy (ML III)
Catabolism
* Aspartylglucosaminuria
  • Fucosidosis
  • mannosidosis
    • Alpha-mannosidosis
    • Beta-mannosidosis
  • Sialidosis
  • Schindler disease
Other
* solute carrier family (Salla disease)
  • Galactosialidosis


Retrieved from "https://wikimd.org/index.php?title=Template:Glycoprotein_disorders&oldid=5695028"
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  • Glycoprotein metabolism disorders
  • Metabolic disorder templates
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  • This page was last edited on 30 April 2024, at 07:55.
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