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Results 1 - 10 of 33 for Glycogen storage disease type 4
  1. Glycogen storage disease type IV 
    ... Glycogen branching enzyme deficiency Glycogen storage disease IV Glycogen storage disease type 4 Glycogenosis 4 Glycogenosis, type IV GSD IV GSD ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-iv - Genetics
  2. GBE1 gene 
    ... the GBE1 gene have been found to cause glycogen storage disease type IV (GSD IV). This disorder is characterized by liver ... Moses SW, Parvari R. The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studies. ...
    https://medlineplus.gov/genetics/gene/gbe1 - Genetics
  3. Glycogen storage disease type I 
    ... 501-8. doi: 10.1007/s00431-005-1657-4. Epub 2005 May 19. Citation on PubMed
    https://medlineplus.gov/.../glycogen-storage-disease-type-i - Genetics
  4. Glycogen storage disease type IX 
    ... Genet A. 2005 Feb 15;133A(1):82-4. doi: 10.1002/ajmg.a.30517. Citation on PubMed
    https://medlineplus.gov/.../glycogen-storage-disease-type-ix - Genetics
  5. Carbohydrate Metabolism Disorders (National Library of Medicine)  
    Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
    https://medlineplus.gov/carbohydratemetabolismdisorders.html - Health Topics
  6. Glycogen storage disease type V 
    ... patients. Hum Mutat. 2007 Feb;28(2):203-4. doi: 10.1002/humu.9474. Citation on PubMed
    https://medlineplus.gov/.../glycogen-storage-disease-type-v - Genetics
  7. Glycogen storage disease type VII 
    ... the PFKM gene. Front Physiol. 2013 Dec 30;4:393. doi: 10.3389/fphys.2013.00393. eCollection 2013. Citation on PubMed or Free article on PubMed Central
    https://medlineplus.gov/.../glycogen-storage-disease-type-vii - Genetics
  8. GAA gene 
    ... glucosidase preproprotein acid maltase Aglucosidase alfa Alpha-1,4-glucosidase Amyloglucosidase Glucoamylase glucosidase, alpha; acid glucosidase, alpha; acid (Pompe disease, glycogen storage disease type II) LYAG LYAG_HUMAN lysosomal alpha-glucosidase Tests ...
    https://medlineplus.gov/genetics/gene/gaa - Genetics
  9. Pompe disease 
    ... maltase deficiency Acid maltase deficiency disease Alpha-1,4-glucosidase deficiency AMD Deficiency of alpha-glucosidase GAA deficiency Glycogen storage disease type II Glycogenosis type II GSD II GSD2 Pompe' ...
    https://medlineplus.gov/genetics/condition/pompe-disease - Genetics
  10. SLC37A4 gene 
    ... CARRIER FAMILY 37 (GLUCOSE-6-PHOSPHATE TRANSPORTER), MEMBER 4; SLC37A4 NCBI Gene ClinVar Chou JY, Jun HS, Mansfield BC. Neutropenia in type Ib glycogen storage disease. Curr Opin Hematol. 2010 Jan;17(1):36- ...
    https://medlineplus.gov/genetics/gene/slc37a4 - Genetics
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