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.
Follow this condition to get notified about new trialsSub-types
Broader categories
Disease
(717)
Metabolic disease
(241)
Hereditary disease
(188)
Inborn errors of metabolism
(47)
Lysosomal storage disease
(36)
Human disease
(15)
Developmental defect during embryogenesis
(8)
Disease of genetic or genomic mechanism
(2)
Developmental anomaly of metabolic origin
(0)
Disease by developmental or physiological process
(0)