Lipiodosis, Table 1. Lipid storage disease
| Gauchers disease (glycosylceramide lipiodosis) |
| Niemann Pick disease (sphingomyelin lipidosis) |
| Fabrys disease (glycolipidosis) |
| Refsums disease (phytanic acid storage disease) |
| Krabbes disease (galactosylceramide lipidosis) |
| Metachromatic leukodystrophy (sulphatide lipidosis) |
| Farber's lipogranulomatosis (ceramidase deficiency) |
| Gangliosidosis |
| Sea-blue histiocytosis |
| Tay Sachs disease |
| Fucosidosis |
The disorders are discussed more fully under their specific names.










