Alpha-N-acetylgalactosaminidase deficiency type 3
MONDO:0019264Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 3 is a rare clinically heterogeneous type of NAGA deficiency with developmental, neurologic and psychiatric manifestations presenting at an intermediate age.
Also known as: NAGA deficiency type 3, Schindler disease type 3
0 clinical trials for this condition and its sub-types.
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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)
Carbohydrate metabolism disease
(4)
Disease of genetic or genomic mechanism
(2)
Inborn carbohydrate metabolic disorder
(2)
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