Sialidosis type 2 (Q97055): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
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). |
Statements
CID11:ID_1855856697
0 references
dki-india-ID_1855856697
0 references
Concluído
0 references
