GM2 gangliosidosis (Q90731): Difference between revisions
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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 |
||
| 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. |
Statements
CID11:ID_1513691830
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dki-india-ID_1513691830
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Concluído
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