Pages that link to "Methylmalonic acidemia"
Jump to navigation
Jump to search
The following pages link to Methylmalonic acidemia:
Displayed 104 items.
- Glucoglycinuria (← links)
- Tyrosinemia (← links)
- Leukopenia (← links)
- Trimethylaminuria (← links)
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- ICD-10 Chapter E (← links)
- List of diseases (M) (← links)
- List of genetic disorders (← links)
- Cholesteryl ester storage disease (← links)
- Batten disease (← links)
- Chromosome 4 (human) (← links)
- Chromosome 6 (human) (← links)
- Chromosome 12 (human) (← links)
- Carbamoyl phosphate synthetase I deficiency (← links)
- Glucose-galactose malabsorption (← links)
- Glutaric aciduria type 1 (← links)
- Glutathione synthetase deficiency (← links)
- Guanidinoacetate methyltransferase deficiency (← links)
- Hyperlysinemia (← links)
- Hypermethioninemia (← links)
- Hyperprolinemia (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- Isovaleric acidemia (← links)
- N-Acetylglutamate synthase deficiency (← links)
- Ornithine transcarbamylase deficiency (← links)
- Ornithine translocase deficiency (← links)
- Prolidase deficiency (← links)
- Pyruvate carboxylase deficiency (← links)
- Sarcosinemia (← links)
- Succinic semialdehyde dehydrogenase deficiency (← links)
- Urea cycle disorder (← links)
- Variegate porphyria (← links)
- Methylmalonyl-CoA mutase (← links)
- Mixed disorder of acid-base balance (← links)
- Inborn error of metabolism (← links)
- Causes of hypoglycemia (← links)
- Disorders of calcium metabolism (← links)
- Reductive acetyl CoA Pathway (← links)
- Entner-Doudoroff Pathway (← links)
- Wikipedia:Wikiproject Metabolic Pathways/templates (← links)
- Glucose-6-phosphate (← links)
- List of fatty acid metabolism disorders (← links)
- Methylmalonic acid (← links)
- Hypotonia (← links)
- Gangliosidosis (← links)
- Growth failure (← links)
- Renal glycosuria (← links)
- Testpage3 (← links)
- Sialidosis (← links)
- Hyperammonemia (← links)
- List of amino acid metabolism disorders (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- Pseudo-Hurler polydystrophy (← links)
- Hepatoerythropoietic porphyria (← links)
- MMA (← links)
- Aspartylglucosaminuria (← links)
- Cystathioninuria (← links)
- ICD-10 Chapter IV: Endocrine, nutritional and metabolic diseases (← links)
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- Chromosome 4 (← links)
- Chromosome 12 (← links)
- Chromosome 6 (← links)
- The Living Textbook of Endocrinology (← links)
- The Living Textbook of Metabolic disorders (← links)
- The WikiDoc Living Textbook of Endocrinology (← links)
- The WikiDoc Living Textbook of Metabolic Disorders (← links)
- ICD-10 Chapter E: Endocrine, nutritional and metabolic diseases (← links)
- Methylmalonic aciduria (redirect page) (← links)
- Hyperreflexia (← links)
- Vitamin B12 (← links)
- Newborn screening (← links)
- Chromosome 4 (human) (← links)
- Methylmalonyl-CoA mutase (← links)
- Propionyl-CoA (← links)
- Chromosome 4 (← links)
- Combined immunodeficiency (← links)
- Thrombocytopenia causes (← links)
- Macrocytic anemia causes (← links)
- Neutropenia causes (← links)
- Coma causes (← links)
- MMADHC (← links)
- MMAB (← links)
- Inborn errors of renal tubular transport (← links)
- Hypervalinemia (← links)
- Organic acidemia (← links)
- Carnosinemia (← links)
- Hawkinsinuria (← links)
- Inborn errors of amino acid metabolism (← links)
- D-Glyceric acidemia (← links)
- Urocanic aciduria (← links)
- Amino acid transport disorder (← links)
- Argininemia (← links)
- 2-Hydroxyglutaric aciduria (← links)
- Type I tyrosinemia (← links)
- Type II tyrosinemia (← links)
- Type III tyrosinemia (← links)
- Cardiac amyloidosis differential diagnosis (← links)
- Methylmalonic Acidemia (redirect page) (← links)
- Coma causes (← links)
- Osteoporosis causes (← links)
- Early myoclonic encephalopathy (← links)
- POEMS syndrome differential diagnosis (← links)
- Metabolic acidosis causes (← links)
- Coma causes (← links)
- Phenylketonuria differential diagnosis (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links)
- Hypertryptophanemia (← links)
- Sandbox:Mental retardation causes (← links)
- MMACHC (← links)
- MMAA (← links)
- Haptocorrin (← links)
- Wild-type (senile) amyloidosis differential diagnosis (← links)
- Primary amyloidosis differential diagnosis (← links)
- Secondary amyloidosis differential diagnosis (← links)
- Familial amyloidosis differential diagnosis (← links)
- Template:Metabolic pathway (← links)
- Template:Metabolic pathology (← links)
- Template:Amino acid metabolic pathology (← links)