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Glycolipidosis

This group of disorders encompasses disturbances in clycolipid synthesis, storage, and transport.

Historical Aspects

The term was coined 1964 in a paper by Minkowitz.[Error: Macro 'ref' doesn't exist]

Systematic

Hereditary metabolic diseases
Coenzyme Q10 deficiency
Congenital disorder of glycosylation
Disorders of cobalamin metabolism
Disorders of iron metabolism
Disorders of urate metabolism
Disturbances in phosphate metabolism
Disturbances of glucose metabolism
Food intolerance
Genetic hyperbilirubinemia
Glycolipidosis
Inclusion body myopathy 2
GNE
Infantile sialic acid storage disorder
SLC17A5
Nonaka myopathy
GNE
Salla disease
SLC17A5
Sialuria
GNE
HADH deficiency
Hereditary disorders protein metabolism
Hereditary lipid disorders
Hypercatabolic hypoproteinemia
Hyperzincemia and hypercalprotectinemia
Hypomagnesemia
Hypomethylation syndrome
Lysosomal storage disease
MELAS syndrome
Methionine adenosyltransferase deficiency
Methylmalonic aciduria
Urea cycle disorders

References:

1.

None (1964) A NEW FORM OF VISCERAL HISTIOCYTIC GLYCOLIPIDOSIS WITH MENTAL RETARDATION.

external link
2.

OMIM.ORG article

Omim 608949 external link
Update: Aug. 14, 2020
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