5C54.Y Other specified congenital disorders of glycosylation and protein modification

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01

Other specified congenital disorders of glycosylation and protein modification
Disorders of glycosphingolipid or glycosylphosphatidylinositol anchor glycosylation
Lactosylceramide alpha-2,3-sialyltransferase deficiency
Infantile-onset symptomatic epilepsy syndrome - developmental stagnation - blindness
GM3 synthase deficiency
Amish infantile epilepsy
Phosphatidylinositolglycan, class M deficiency
PIGM deficiency
Disorders of protein ubiquitinylation
Other specified disorders of protein modification

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