Mucolipidosis
MONDO:0019248A group of inherited lysosomal storage diseases characterized by accumulation of lipids and carbohydrates in the tissues, resulting in mental disabilities and skeletal malformations.
5 clinical trials for this condition and its sub-types, 4 tagged with Mucolipidosis itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Mucolipidosis
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Familial mucolipidosis 0 trials · 5 incl. sub-types
5 sub-types
- Mucolipidosis type IV 3 trials
- Sialidosis type 1 2 trials
- GNPTG-mucolipidosis 0 trials
- Mucolipidosis type III, alpha/beta 0 trials
- Sialidosis type 2 0 trials Sub-types →
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GNPTAB-mucolipidosis 0 trials
2 sub-types
- Mucolipidosis type II 0 trials
- Mucolipidosis type III, alpha/beta 0 trials