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- Transaldolase_deficiency abstract "Transaldolase deficiency is a disease characterised by abnormally low levels of the Transaldolase enzyme. It is a metabolic enzyme involved in the pentose phosphate pathway. It is caused by mutation in the transaldolase gene (TALDO1). It was first described by Verhoeven et al. in 2001.".
- Transaldolase_deficiency omim "606003".
- Transaldolase_deficiency thumbnail Transaldolaseribbon.jpg?width=300.
- Transaldolase_deficiency wikiPageID "18859352".
- Transaldolase_deficiency wikiPageLength "10094".
- Transaldolase_deficiency wikiPageOutDegree "25".
- Transaldolase_deficiency wikiPageRevisionID "679130075".
- Transaldolase_deficiency wikiPageWikiLink Category:Inborn_errors_of_carbohydrate_metabolism.
- Transaldolase_deficiency wikiPageWikiLink Cirrhosis.
- Transaldolase_deficiency wikiPageWikiLink Coagulopathy.
- Transaldolase_deficiency wikiPageWikiLink Cutis_laxa.
- Transaldolase_deficiency wikiPageWikiLink D-erythrose_4-phosphate.
- Transaldolase_deficiency wikiPageWikiLink D-glyceraldehyde_3-phosphate.
- Transaldolase_deficiency wikiPageWikiLink Erythrose_4-phosphate.
- Transaldolase_deficiency wikiPageWikiLink Fructose_6-phosphate.
- Transaldolase_deficiency wikiPageWikiLink Glucose-6-phosphate_dehydrogenase_deficiency.
- Transaldolase_deficiency wikiPageWikiLink Glucose_6-phosphate.
- Transaldolase_deficiency wikiPageWikiLink Glyceraldehyde_3-phosphate.
- Transaldolase_deficiency wikiPageWikiLink Hepatosplenomegaly.
- Transaldolase_deficiency wikiPageWikiLink Inborn_error_of_metabolism.
- Transaldolase_deficiency wikiPageWikiLink Liver_cirrhosis.
- Transaldolase_deficiency wikiPageWikiLink Pentose_phosphate_pathway.
- Transaldolase_deficiency wikiPageWikiLink Polyol.
- Transaldolase_deficiency wikiPageWikiLink Polyols.
- Transaldolase_deficiency wikiPageWikiLink Ribose_5-phosphate.
- Transaldolase_deficiency wikiPageWikiLink Sedoheptulose_7-phosphate.
- Transaldolase_deficiency wikiPageWikiLink Spermatozoa.
- Transaldolase_deficiency wikiPageWikiLink Spermatozoon.
- Transaldolase_deficiency wikiPageWikiLink Thrombocytopenia.
- Transaldolase_deficiency wikiPageWikiLink Transaldolase.
- Transaldolase_deficiency wikiPageWikiLink File:Transaldolase_annotated_PENTOSE_PHOSPHATE_Pathway.gif.
- Transaldolase_deficiency wikiPageWikiLink File:Transaldolaseribbon.jpg.
- Transaldolase_deficiency wikiPageWikiLinkText "Transaldolase deficiency".
- Transaldolase_deficiency caption "Transaldolase deficiency results from a change in the proteins formation due to deletion of residue Ser171 or a replacement of Arg192 by His or Cys".
- Transaldolase_deficiency hasPhotoCollection Transaldolase_deficiency.
- Transaldolase_deficiency name "Transaldolase deficiency".
- Transaldolase_deficiency omim "606003".
- Transaldolase_deficiency wikiPageUsesTemplate Template:Inborn_errors_of_carbohydrate_metabolism.
- Transaldolase_deficiency wikiPageUsesTemplate Template:Infobox_disease.
- Transaldolase_deficiency wikiPageUsesTemplate Template:Reflist.
- Transaldolase_deficiency subject Category:Inborn_errors_of_carbohydrate_metabolism.
- Transaldolase_deficiency hypernym Disease.
- Transaldolase_deficiency type Disease.
- Transaldolase_deficiency type Error.
- Transaldolase_deficiency type Thing.
- Transaldolase_deficiency type Q12136.
- Transaldolase_deficiency comment "Transaldolase deficiency is a disease characterised by abnormally low levels of the Transaldolase enzyme. It is a metabolic enzyme involved in the pentose phosphate pathway. It is caused by mutation in the transaldolase gene (TALDO1). It was first described by Verhoeven et al. in 2001.".
- Transaldolase_deficiency label "Transaldolase deficiency".
- Transaldolase_deficiency sameAs m.04gqbln.
- Transaldolase_deficiency sameAs Q7833752.
- Transaldolase_deficiency sameAs Q7833752.
- Transaldolase_deficiency wasDerivedFrom Transaldolase_deficiency?oldid=679130075.
- Transaldolase_deficiency depiction Transaldolaseribbon.jpg.
- Transaldolase_deficiency isPrimaryTopicOf Transaldolase_deficiency.
- Transaldolase_deficiency name "Transaldolase deficiency".