Inborn aminoacylase deficiency
MONDO:0017686An inherited metabolic disease that is has its basis in the disruption of aminoacylase activity.
Also known as: inborn aminoacylase activity disorder, inborn error of aminoacylase activity, rare inborn error of aminoacylase activity, aminoacylase deficiency
6 clinical trials for this condition and its sub-types, 0 tagged with Inborn aminoacylase deficiency itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Inborn aminoacylase deficiency
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Canavan disease 6 trials
2 sub-types
- Mild Canavan disease 0 trials
- Severe Canavan disease 0 trials
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Aminoacylase 1 deficiency 0 trials
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.