Metabolic disorders
Metabolic disorders ( Sub Categories )
Congenital disorder of glycosylation
Congenital disorders of glycosylation (CDG) are a group of rare genetic diseases that affect the process of attaching sugars to proteins and lipids, leading to various organ dysfunctions
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Disorder of biogenic amine metabolism and transport
Biological Amines Metabolism and Transport Disorder is a defect in breaking down or transporting nitrogen-containing organic compounds, leading to the buildup of harmful substances in the body and causing issues in the nervous system and growth.
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Disorder of energy metabolism
Energy metabolism disorders are conditions that affect the body's ability to produce or utilize energy due to metabolic pathway defects, potentially causing fatigue, muscle weakness, or organ dysfunction.
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Disorder of lipid metabolism
Lipid metabolism disorder is a condition affecting the breakdown or storage of fats in the body, potentially leading to energy deficiencies, fat accumulation in organs, or metabolic imbalances.
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Disorder of lysosomal-related organelles
Lysosome-related organelle disorder is a rare condition affecting the function of lysosomes and associated organelles, potentially leading to immune dysfunction, pigmentation issues, and neurological or cellular disorders.
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Disorder of metabolite absorption and transport
Metabolite absorption and transport disorder is a condition affecting the body's ability to absorb or transport essential metabolic compounds, potentially leading to malnutrition, energy deficiencies, and growth or cellular function disorders.
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