Alpha-N-acetylgalactosaminidase deficiency type 1 (Q97052): Difference between revisions
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| description / pt-br | description / pt-br | ||
A deficiência de alfa-N-acetilgalactosaminidase (NAGA) tipo 1 é um tipo muito raro e grave de deficiência de NAGA caracterizada por distrofia neuroaxonal infantil. | |||
| description / en | description / en | ||
Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 1 is a very rare and severe type of NAGA deficiency characterised by infantile neuroaxonal dystrophy. | |||
Revision as of 13:05, 16 August 2026
Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 1 is a very rare and severe type of NAGA deficiency characterised by infantile neuroaxonal dystrophy.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1058486825 |
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| English | Alpha-N-acetylgalactosaminidase deficiency type 1 |
Alpha-N-acetylgalactosaminidase (NAGA) deficiency type 1 is a very rare and severe type of NAGA deficiency characterised by infantile neuroaxonal dystrophy. |
