Sialidosis type 2 (Q97055): Difference between revisions

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Latest 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
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).