Many disorders of metabolism have a genetic component, or are presumed to do so, with research being directed at finding the factors responsible.
Subcategories 40
- Alkaptonuria
- Alpha-1 Antitrypsin Deficiency
- Amyloidosis
- Aspartylglucosaminuria
- Celiac Disease
- Congenital Chloride Diarrhea
- Crigler-Najjar Syndrome
- Cystinosis
- Familial Hypercholesterolemia
- Fatty Oxidation Disorders
- GRACILE Syndrome
- Gilbert's Syndrome
- Gilbert's Syndrome
- Glutaricaciduria
- Glycogen Storage Disease Type I
- Glycogen Storage Disease Type II
- Hemochromatosis
- Hurler Syndrome
- Lactose Intolerance
- Lesch-Nyhan Syndrome
- Lowe Syndrome
- Lysinuric Protein Intolerance
- Madelung's Disease
- Mannosidosis
- Maple Syrup Urine Disease
- McArdle's
- McArdle's
- Metabolic Brain Diseases
- Mucolipidosis
- Mucopolysaccharidoses
- Nonketotic Hyperglycinemia
- Opitz Syndrome
- Phenylketonuria
- Porphyrias
- Propionic Acidemia
- Sanfilippo Syndrome
- Smith Lemli Opitz Syndrome
- Trimethylaminuria
- Tyrosinemia
- Zellweger Syndrome
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