Niemann-Pick disease
MONDO:0001982A group of inherited, severe metabolic disorders in which sphingomyelin accumulates in lysosomes in cells. The lysosomes normally transport material through and out of the cell.
Also known as: Niemann-Pick disease with cholesterol esterification block, Niemann-Pick disease, subacute juvenile form, lipoid histiocytosis (classical phosphatide), sphingomyelin/cholesterol lipidosis, type A Niemann-Pick disease
29 clinical trials for this condition and its sub-types, 10 tagged with Niemann-Pick disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Niemann-Pick disease
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Niemann-Pick disease type C 12 trials · 13 incl. sub-types
7 sub-types
- Niemann-Pick disease, type C1 2 trials
- Niemann-Pick disease, type C2 1 trial
- Niemann-Pick disease type C, adult neurologic onset 0 trials
- Niemann-Pick disease type C, juvenile neurologic onset 0 trials
- Niemann-Pick disease type C, late infantile neurologic onset 0 trials
- Niemann-Pick disease type C, severe early infantile neurologic onset 0 trials
- Niemann-Pick disease type C, severe perinatal form 0 trials
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Acid sphingomyelinase deficiency 7 trials · 10 incl. sub-types
2 sub-types
- Niemann-Pick disease type A 4 trials
- Niemann-Pick disease type B 1 trial
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Niemann-Pick disease type E 0 trials