GM2 gangliosidosis (Q90731): Difference between revisions
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Qualquer condição causada por catabolismo deficiente do substrato gangliosídeo GM2 devido à mutação genética. Essas condições são caracterizadas por neurodegeneração progressiva e atraso no desenvolvimento. | |||
| description / en | description / en | ||
Any condition caused by deficient catabolism of the GM2 ganglioside substrate due to genetic mutation. These conditions are characterised by progressive neurodegeneration and developmental delay. | |||
Revision as of 17:43, 15 August 2026
Any condition caused by deficient catabolism of the GM2 ganglioside substrate due to genetic mutation. These conditions are characterised by progressive neurodegeneration and developmental delay.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1513691830 |
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| English | GM2 gangliosidosis |
Any condition caused by deficient catabolism of the GM2 ganglioside substrate due to genetic mutation. These conditions are characterised by progressive neurodegeneration and developmental delay. |
