Glycogen storage disease due to phosphoglycerate kinase 1 deficiency (Q84807): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_1396572570 | |||
| Property / Canary Token: dki-india-ID_1396572570 / rank | |||
Normal rank | |||
Revision as of 10:09, 15 August 2026
Phosphoglycerate kinase (PGK) deficiency is an inborn error of metabolism characterised by variable combinations of nonspherocytic haemolytic anaemia, myopathy, and various central nervous system abnormalities.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1396572570 |
||
| English | Glycogen storage disease due to phosphoglycerate kinase 1 deficiency |
Phosphoglycerate kinase (PGK) deficiency is an inborn error of metabolism characterised by variable combinations of nonspherocytic haemolytic anaemia, myopathy, and various central nervous system abnormalities. |
Statements
CID11:ID_1396572570
0 references
dki-india-ID_1396572570
0 references
