Logo
Unionpedia
Communication
Get it on Google Play
New! Download Unionpedia on your Android™ device!
Install
Faster access than browser!
 

Glycogen storage disease and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Shortcuts: Differences, Similarities, Jaccard Similarity Coefficient, References.

Difference between Glycogen storage disease and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Glycogen storage disease vs. ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

A glycogen storage disease (GSD, also glycogenosis and dextrinosis) is a metabolic disorder caused by enzyme deficiencies affecting either glycogen synthesis, glycogen breakdown or glycolysis (glucose breakdown), typically within muscles and/or liver cells. This is an overview about the chapter IV (also called chapter E) of the International Statistical Classification of Diseases and Related Health Problems 10th Revision (ICD-10).

Similarities between Glycogen storage disease and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases

Glycogen storage disease and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases have 11 things in common (in Unionpedia): Glycogen storage disease type I, Glycogen storage disease type II, Glycogen storage disease type III, Glycogen storage disease type IV, Glycogen storage disease type V, Hyperlipidemia, Hyperuricemia, Hypoglycemia, Inborn errors of metabolism, Lactic acidosis, Metabolic disorder.

Glycogen storage disease type I

Glycogen storage disease type I (GSD I) or von Gierke disease, is the most common of the glycogen storage diseases.

Glycogen storage disease and Glycogen storage disease type I · Glycogen storage disease type I and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Glycogen storage disease type II

Glycogen storage disease type II, also called Pompe disease, is an autosomal recessive metabolic disorder which damages muscle and nerve cells throughout the body.

Glycogen storage disease and Glycogen storage disease type II · Glycogen storage disease type II and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Glycogen storage disease type III

Glycogen storage disease type III is an autosomal recessive metabolic disorder and inborn error of metabolism (specifically of carbohydrates) characterized by a deficiency in glycogen debranching enzymes.

Glycogen storage disease and Glycogen storage disease type III · Glycogen storage disease type III and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Glycogen storage disease type IV

Glycogen storage disease type IV, also known as Andersen’s Disease, is a form of glycogen storage disease, which is caused by an inborn error of metabolism.

Glycogen storage disease and Glycogen storage disease type IV · Glycogen storage disease type IV and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Glycogen storage disease type V

Glycogen storage disease type V (GSD-V) is a metabolic disorder, more specifically a glycogen storage disease, caused by a deficiency of myophosphorylase.

Glycogen storage disease and Glycogen storage disease type V · Glycogen storage disease type V and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Hyperlipidemia

Hyperlipidemia is abnormally elevated levels of any or all lipids or lipoproteins in the blood.

Glycogen storage disease and Hyperlipidemia · Hyperlipidemia and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Hyperuricemia

Hyperuricemia is an abnormally high level of uric acid in the blood.

Glycogen storage disease and Hyperuricemia · Hyperuricemia and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Hypoglycemia

Hypoglycemia, also known as low blood sugar, is when blood sugar decreases to below normal levels.

Glycogen storage disease and Hypoglycemia · Hypoglycemia and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases · See more »

Inborn errors of metabolism

Inborn errors of metabolism form a large class of genetic diseases involving congenital disorders of metabolism.

Glycogen storage disease and Inborn errors of metabolism · ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases and Inborn errors of metabolism · See more »

Lactic acidosis

Lactic acidosis is a medical condition characterized by the buildup of lactate (especially L-lactate) in the body, which results in an excessively low pH in the bloodstream.

Glycogen storage disease and Lactic acidosis · ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases and Lactic acidosis · See more »

Metabolic disorder

A metabolic disorder can happen when abnormal chemical reactions in the body alter the normal metabolic process.

Glycogen storage disease and Metabolic disorder · ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases and Metabolic disorder · See more »

The list above answers the following questions

Glycogen storage disease and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases Comparison

Glycogen storage disease has 80 relations, while ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases has 388. As they have in common 11, the Jaccard index is 2.35% = 11 / (80 + 388).

References

This article shows the relationship between Glycogen storage disease and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases. To access each article from which the information was extracted, please visit:

Hey! We are on Facebook now! »