Curlie - Health: Conditions and Diseases: Nutritional and Metabolic Disorders: Inherited

Inherited

Many disorders of metabolism have a genetic component, or are presumed to do so, with research being directed at finding the factors responsible.
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Subcategories 40

Alpha-1 Antitrypsin Deficiency

Aspartylglucosaminuria

Congenital Chloride Diarrhea

Crigler-Najjar Syndrome

Familial Hypercholesterolemia

Fatty Oxidation Disorders

Gilbert's Syndrome

Gilbert's Syndrome

Glutaricaciduria

Glycogen Storage Disease Type I

Glycogen Storage Disease Type II

GRACILE Syndrome

Hemochromatosis

Hurler Syndrome

Lactose Intolerance

Lesch-Nyhan Syndrome

Lysinuric Protein Intolerance

Madelung's Disease

Maple Syrup Urine Disease

Metabolic Brain Diseases

Mucopolysaccharidoses

Nonketotic Hyperglycinemia

Phenylketonuria

Propionic Acidemia

Sanfilippo Syndrome

Smith Lemli Opitz Syndrome

Trimethylaminuria

Zellweger Syndrome

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Last update:

March 27, 2025 at 22:40:34 UTC

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