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Sphingolipidosis

An inherited metabolic disorder that affects the lysosomal degradation of the spinhgolipids. Representative examples include Gaucher disease, Tay-Sachs disease, and Niemann-Pick disease.

6 trials tagged with this condition →

Fabry disease 64 trials
Gaucher disease 46 trials Sub-types →
Gangliosidosis 3 trials · 24 incl. sub-types Sub-types →
Niemann-Pick disease 10 trials · 22 incl. sub-types Sub-types →
Metachromatic leukodystrophy 20 trials Sub-types →
Krabbe disease 15 trials Sub-types →
Mucosulfatidosis 4 trials
ASAH1-related sphingolipidosis 0 trials · 1 incl. sub-types Sub-types →
PSAP-related sphingolipidosis 0 trials · 1 incl. sub-types Sub-types →
Autosomal recessive cerebellar ataxia with late-onset spasticity 0 trials
Sea-blue histiocyte syndrome 0 trials