The following pages link to Methylmalonic acidemia
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Hypoglycemia (links | edit)
- Phenylketonuria (links | edit)
- List of genetic disorders (links | edit)
- Methionine (links | edit)
- Isoleucine (links | edit)
- Threonine (links | edit)
- Valine (links | edit)
- Vitamin deficiency (links | edit)
- Alkaptonuria (links | edit)
- Macrocephaly (links | edit)
- List of diseases (M) (links | edit)
- MMA (disambiguation) (links | edit)
- Methylmalonic acidemias (links | edit)
- Propionic acidemia (links | edit)
- Hyperammonemia (links | edit)
- Malonic acid (links | edit)
- Waardenburg syndrome (links | edit)
- Homocystinuria (links | edit)
- Newborn screening (links | edit)
- Hypotonia (links | edit)
- Cystinuria (links | edit)
- Ornithine transcarbamylase deficiency (links | edit)
- Inborn errors of metabolism (links | edit)
- Trimethylaminuria (links | edit)
- Isovaleric acidemia (links | edit)
- Maple syrup urine disease (links | edit)
- Cystinosis (links | edit)
- Citrullinemia (links | edit)
- Holocarboxylase synthetase deficiency (links | edit)
- Beta-ketothiolase deficiency (links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (links | edit)
- Tyrosinemia (links | edit)
- Microtia (links | edit)
- Hartnup disease (links | edit)
- Glutaric aciduria type 1 (links | edit)
- Saccharopinuria (links | edit)
- Ochronosis (links | edit)
- Lysinuric protein intolerance (links | edit)
- Hyperlysinemia (links | edit)
- Biotinidase deficiency (links | edit)
- Pantothenate kinase-associated neurodegeneration (links | edit)
- Chromosome 6 (links | edit)
- Chromosome 4 (links | edit)
- Chromosome 12 (links | edit)
- Tetrahydrobiopterin deficiency (links | edit)
- Hermansky–Pudlak syndrome (links | edit)
- Argininosuccinic aciduria (links | edit)
- Oculocutaneous albinism (links | edit)
- Glutaric acidemia type 2 (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)