Pages that link to "Biotinidase deficiency"
Showing 50 items.
- Adrenoleukodystrophy (links | edit)
- Biotin (links | edit)
- List of genetic disorders (links | edit)
- Hair loss (links | edit)
- List of diseases (B) (links | edit)
- Lactic acidosis (links | edit)
- Methylmalonic acidemias (links | edit)
- Propionic acidemia (links | edit)
- Medium-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
- Newborn screening (links | edit)
- Inborn errors of metabolism (links | edit)
- Fatty acid metabolism (links | edit)
- Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (links | edit)
- Holocarboxylase synthetase deficiency (links | edit)
- Beta oxidation (links | edit)
- Systemic primary carnitine deficiency (links | edit)
- Inborn error of lipid metabolism (links | edit)
- Carnitine palmitoyltransferase I deficiency (links | edit)
- Carnitine palmitoyltransferase II deficiency (links | edit)
- Β-Hydroxy β-methylbutyric acid (links | edit)
- Carnitine-acylcarnitine translocase deficiency (links | edit)
- Mitochondrial trifunctional protein deficiency (links | edit)
- Very long-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
- Biotinidase deficiency (transclusion) (links | edit)
- Delayed milestone (links | edit)
- Pantothenate kinase-associated neurodegeneration (links | edit)
- Chromosome 3 (links | edit)
- Tetrahydrobiopterin deficiency (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)
- Malonic aciduria (links | edit)
- 6-Pyruvoyltetrahydropterin synthase deficiency (links | edit)
- Short-chain acyl-coenzyme A dehydrogenase deficiency (links | edit)
- 2,4 Dienoyl-CoA reductase deficiency (links | edit)
- 3-Methylcrotonyl-CoA carboxylase deficiency (links | edit)
- Causes of autism (links | edit)
- List of MeSH codes (C18) (links | edit)
- List of MeSH codes (C16) (links | edit)
- Carboxylase Deficiency, Multiple, Late-Onset (redirect page) (links | edit)
- Sjögren–Larsson syndrome (links | edit)
- Acute fatty liver of pregnancy (links | edit)
- Familial isolated vitamin E deficiency (links | edit)
- 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (links | edit)
- Biotinidase (links | edit)
- Biotin deficiency (links | edit)
- Congenital disorders of amino acid metabolism (links | edit)
- Multiple carboxylase deficiency (links | edit)
- Metabolic myopathy (links | edit)
- Molybdenum cofactor deficiency (links | edit)
- Fatty-acid metabolism disorder (links | edit)