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.
6 clinical trials for this condition and its sub-types, 5 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 · 6 incl. sub-types
5 sub-types
- Mucolipidosis type IV 4 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
Most studied deeper sub-types
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Scientists track rare brain diseases to unlock clues for future treatments
Knowledge-focused Recruiting nowThis study follows people with rare genetic disorders that cause harmful substances to build up in the body, leading to brain damage. Researchers will monitor up to 200 participants over time using exams, surveys, and lab tests. The goal is to better understand how these diseases…
Sponsor: National Human Genome Research Institute (NHGRI) • Aim: Knowledge-focused
Last updated Nov 07, 2026 00:00 UTC
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Coordination of rare diseases at sanford
Recruiting nowThe Coordination of Rare Diseases at Sanford (CoRDS) is an international patient registry that serves as a centralized resource for rare disease research. Individuals affected by rare diseases, undiagnosed conditions, and disorders of unknown prevalence may voluntarily contribute…
Sponsor: Sanford Health
Last updated Oct 30, 2026 00:00 UTC