Sialidosis type 2 (Q97055): Difference between revisions
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Revision as of 13:05, 16 August 2026
Sialidosis is a lysosomal storage disease belonging to the group of oligosaccharidoses or glycoproteinoses. Two types of sialidosis have been defined, type 2 (also referred to as the infantile, dysmorphic form of sialidosis) and type 1 (a later onset form without major dysmorphic features).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1855856697 |
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| English | Sialidosis type 2 |
Sialidosis is a lysosomal storage disease belonging to the group of oligosaccharidoses or glycoproteinoses. Two types of sialidosis have been defined, type 2 (also referred to as the infantile, dysmorphic form of sialidosis) and type 1 (a later onset form without major dysmorphic features). |
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CID11:ID_1855856697
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