2. Glycogen storage disease type V - Genetics Home Reference
Glycogen storage disease type V (also known as GSDV or McArdle disease) is an inherited disorder caused by an inability to break down a complex sugar called glycogen in muscle cells. A lack of ...
MedlinePlus (Offsite)

3. Glycogen Storage Disease Type VI -- GeneReviews -- NCBI Bookshelf
by either a US CLIA-licensed laboratory or a non-US clinical laboratory. GeneTests does not verify laboratory-submitted information or warrant any aspect of a laboratory's licensure or performance. Clinicians must communicate directly with the lab...
MedlinePlus (Offsite)

4. Glycogen storage disease type V - References - Genetics Home Reference
These sources were used to develop the Genetics Home Reference condition summary on glycogen storage disease type V.
MedlinePlus (Offsite)

5. Hyperlipoproteinemia Type IV
Carbohydrate-Induced Hyperlipemia; Hypercholesterolemia, Type IV; Hyperlipidemia IV; Hyperprebeta-Lipoproteinemia;
Healthline.com (OMS Preferred Provider)

6. Mucolipidosis type IV - Genetics Home Reference
Mucolipidosis type IV is an inherited disorder characterized by delayed development and progressive vision loss. The severe form of the disorder is called typical mucolipidosis type IV, and the mild form is called...
MedlinePlus (Offsite)

7. Mucopolysaccharidosis type IV - Genetics Home Reference
Mucopolysaccharidosis type IV (MPS IV), also known as Morquio syndrome, is a progressive condition that mainly affects the skeleton. The rate at which symptoms worsen varies among affected individuals.
MedlinePlus (Offsite)

8. CDC Features - Hemochromatosis (Iron Storage Disease) Awareness
Hemochromatosis (iron storage disease) occurs when the body absorbs too much iron from foods (and other sources such as vitamins containing iron). If this iron buildup is untreated, it can, over many years, damage the body's organs. Learn the symp...
Centers for Disease Control and Prevention

9. Glycogen Storage Disease, Type IV: eMedicine Endocrinology
A glycogen storage disease (GSD) is the result of an enzyme defect. These enzymes normally catalyze reactions that ultimately convert glycogen compounds to glucose. Enzyme deficiency results in glycogen accumulation...
emedicine.medscape.com

10. Glycogen storage disease type 2
Pompe disease; Acid maltase deficiency disease; Aglucosidase alfa; Alpha-1,4-glucosidase deficiency; Cardiomegalia glycogenica diffusa; Deficiency of alpha-glucosidase; GSD II; Deficiency of lysosomal alpha-glucosidase;
rarediseases.info.nih.gov