Disorders of sphingolipid metabolism and other lipid storage disorders
Notes: Adult GM2 gangliosidosis ; Juvenile GM2 gangliosidosis ; Gangliosidosis NOS ; GM1 gangliosidosis ; GM3 gangliosidosis ; Acid sphingomyelinase deficiency (ASMD) ; Acid sphingomyelinase deficiency type A (ASMD type A) ; Infantile neurovisceral acid sphingomyelinase deficiency ; Acid sphingomyelinase deficiency type B (ASMD type B) ; Chronic visceral acid sphingomyelinase deficiency ; Acid sphingomyelinase deficiency type A/B (ASMD type A/B) ; Chronic neurovisceral acid sphingomyelinase deficiency ; Acid sphingomyelinase deficiency (ASMD) NOS ; Multiple sulfatase deficiency (MSD) ; Farber’s syndrome ; Sulfatide lipidosis ; Batten disease ; Bielschowsky-Jansky disease ; Kufs disease ; Spielmeyer-Vogt disease ; Cerebrotendinous cholesterosis [van Bogaert-Scherer-Epstein] ; Wolman’s disease ; mucolipidosis, types I-III (E77.0-E77.1) ; Refsum’s disease (G60.1) ; adrenoleukodystrophy [Addison-Schilder] (E71.528)