Alpha-N-acetylgalactosaminidase deficiency type 1

MONDO:0012221

Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 1 is a very rare and severe type of NAGA deficiency characterized by infantile neuroaxonal dystrophy.

Also known as: NAGA deficiency type 1, Schindler disease type 1, Schindler disease, type III, Alpha-N-acetylgalactosaminidase deficiency, type 1, Alpha-N-acetylgalactosaminidase deficiency, type 3, N-acetyl-alpha-D-galactosaminidase deficiency type III, NAGA deficiency, type 1, NAGA deficiency, type 3

0 clinical trials for this condition and its sub-types, 0 tagged with Alpha-N-acetylgalactosaminidase deficiency type 1 itself.

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Including sub-types (0) Tagged with Alpha-N-acetylgalactosaminidase deficiency type 1 (0)

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