GM1 gangliosidosis type 2 (Q104019): Difference between revisions
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Revision as of 09:50, 17 August 2026
GM1 gangliosidosis type 2 is a clinically variable, infancy or childhood-onset form of GM1 gangliosidosis characterised by normal early development and psychomotor regression between seven months and three years of age.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1132250614 |
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| English | GM1 gangliosidosis type 2 |
GM1 gangliosidosis type 2 is a clinically variable, infancy or childhood-onset form of GM1 gangliosidosis characterised by normal early development and psychomotor regression between seven months and three years of age. |
