Category: E75 - Disorders of sphingolipid metabolism and other lipid storage disorders
Chapter Notes
Section Notes
Disorders of sphingolipid metabolism and other lipid storage disorders
mucolipidosis, types I-III (E77.0-E77.1)
Refsum's disease (G60.1)
GM2 gangliosidosis
GM2 gangliosidosis, unspecified
Sandhoff disease
Tay-Sachs disease
Other GM2 gangliosidosis
Adult GM2 gangliosidosis
Juvenile GM2 gangliosidosis
Other and unspecified gangliosidosis
Unspecified gangliosidosis
Gangliosidosis NOS
Mucolipidosis IV
Other gangliosidosis
GM1 gangliosidosis
GM3 gangliosidosis
Other sphingolipidosis
adrenoleukodystrophy [Addison-Schilder] (E71.528)
Fabry (-Anderson) disease
Gaucher disease
Krabbe disease
Niemann-Pick disease
Acid sphingomyelinase deficiency (ASMD)
Niemann-Pick disease type A
Acid sphingomyelinase deficiency type A (ASMD type A)
Infantile neurovisceral acid sphingomyelinase deficiency
Niemann-Pick disease type B
Acid sphingomyelinase deficiency type B (ASMD type B)
Chronic visceral acid sphingomyelinase deficiency
Niemann-Pick disease type C
Niemann-Pick disease type D
Niemann-Pick disease type A/B
Acid sphingomyelinase deficiency type A/B (ASMD type A/B)
Chronic neurovisceral acid sphingomyelinase deficiency
Other Niemann-Pick disease
Niemann-Pick disease, unspecified
Acid sphingomyelinase deficiency (ASMD) NOS
Metachromatic leukodystrophy
Sulfatase deficiency
Multiple sulfatase deficiency (MSD)
Farber's syndrome
Sulfatide lipidosis
Sphingolipidosis, unspecified
Neuronal ceroid lipofuscinosis
Batten disease
Bielschowsky-Jansky disease
Kufs disease
Spielmeyer-Vogt disease
Other lipid storage disorders
Cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein]
Wolman's disease
Lipid storage disorder, unspecified
