Glycogen storage disease due to liver glycogen phosphorylase deficiency (Q84793): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||||||||||||||
| Property / Collection date | |||||||||||||||
13 August 2026
| |||||||||||||||
| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 10:08, 15 August 2026
Liver phosphorylase deficiency, or glycogen storage disease type 6b (Hers disease, GSD 6b) is a benign and rare form of glycogen storage disease characterised by hepatomegaly and growth delay, with hypoglycaemic episodes being mild or absent.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1656693213 |
||
| English | Glycogen storage disease due to liver glycogen phosphorylase deficiency |
Liver phosphorylase deficiency, or glycogen storage disease type 6b (Hers disease, GSD 6b) is a benign and rare form of glycogen storage disease characterised by hepatomegaly and growth delay, with hypoglycaemic episodes being mild or absent. |
Statements
CID11:ID_1656693213
0 references
dki-india-ID_1656693213
0 references
Concluído
0 references
13 August 2026
0 references
