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 ·
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 ·
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 ·
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 ·
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 ·
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 ·
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 ·
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 ·
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 ·
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 ·
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 ·
The list above answers the following questions
- What Glycogen storage disease and ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases have in common
- What are the 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 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
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