6-phosphogluconate dehydrogenase deficiency: Difference between revisions
Appearance
Content deleted Content added
m adding orphan template; no mainspace non-redirect non-disambig links using AWB |
Amended stub to more specific & added ICD10 code to infobox |
||
Line 5: | Line 5: | ||
| Caption = |
| Caption = |
||
| DiseasesDB = |
| DiseasesDB = |
||
| ICD10 = |
| ICD10 = {{ICD10|D|55|0|d|55}} |
||
| ICD9 = |
| ICD9 = |
||
| ICDO = |
| ICDO = |
||
Line 23: | Line 23: | ||
{{disease-stub}} |
{{blood-disease-stub}} |
Revision as of 09:37, 22 June 2009
6-phosphogluconate dehydrogenase deficiency |
---|
6-Phosphogluconate dehydrogenase deficiency is a hereditary disease characterised by abnormally low levels of the 6-phosphogluconate dehydrogenase enzyme (abbreviated 6PGD). It is a metabolic enzyme involved in the pentose phosphate pathway, especially important in red blood cell metabolism.
{{Diseases of RBCs and megakaryocytes}} may refer to:
- {{Diseases of RBCs}}, a navigational template for diseases of red blood cells
- {{Diseases of megakaryocytes}}, a navigational template for diseases of clotting
{{Template disambiguation}} should never be transcluded in the main namespace.