Pages that link to "Methylmalonic acidemias"
Showing 13 items.
- Methylmalonic aciduria (redirect page) (links | edit)
- Chromosome 4 (links | edit)
- Methylmalonyl-CoA mutase (links | edit)
- Propionyl-CoA (links | edit)
- Vitamin B12 (links | edit)
- MMAB (links | edit)
- MMADHC (links | edit)
- List of disorders included in newborn screening programs (links | edit)
- Sepiapterin reductase deficiency (links | edit)
- User:Manasa Shetty/sandbox (links | edit)
- Methylmalonic acid (links | edit)
- Combined malonic and methylmalonic aciduria (links | edit)
- Defect in synthesis of adenosylcobalamin (redirect page) (links | edit)
- Methylmalonic acidemia with homocystinuria (redirect page) (links | edit)
- Methylmalonic aciduria microcephaly cataract (redirect page) (links | edit)
- Methylmalonicacidemia with homocystinuria, cbl D (redirect page) (links | edit)
- Methylmalonicaciduria with homocystinuria, cbl F (redirect page) (links | edit)
- Methylmalonicaciduria, vitamin B12 unresponsive, mut-0 (redirect page) (links | edit)
- Vitamin B12 responsive methylmalonic acidemia, cbl A (redirect page) (links | edit)
- Vitamin B12 responsive methylmalonicaciduria (redirect page) (links | edit)
- Methylmalonic acidemia (redirect page) (links | edit)
- 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)
- 2-Hydroxyglutaric aciduria (links | edit)
- Malonic aciduria (links | edit)
- 3-Methylglutaconic aciduria (links | edit)
- 6-Pyruvoyltetrahydropterin synthase deficiency (links | edit)
- 3-Methylcrotonyl-CoA carboxylase deficiency (links | edit)
- Methylmalonyl-CoA mutase deficiency (links | edit)
- Glycine encephalopathy (links | edit)
- Hawkinsinuria (links | edit)
- Fumarase deficiency (links | edit)
- William Nyhan (links | edit)
- Aminoaciduria (links | edit)
- Oculocerebrorenal syndrome (links | edit)
- 2-Methylbutyryl-CoA dehydrogenase deficiency (links | edit)
- Histidinemia (links | edit)
- Succinic semialdehyde dehydrogenase deficiency (links | edit)
- N-Acetylglutamate synthase deficiency (links | edit)
- Hyperhomocysteinemia (links | edit)
- Methylmalonyl-CoA mutase (links | edit)
- Isobutyryl-coenzyme A dehydrogenase deficiency (links | edit)
- Carbamoyl phosphate synthetase I deficiency (links | edit)
- Ethylmalonic encephalopathy (links | edit)
- Sarcosinemia (links | edit)
- Familial isolated vitamin E deficiency (links | edit)
- Ornithine translocase deficiency (links | edit)
- Hydroxocobalamin (links | edit)
- Prolidase deficiency (links | edit)
- Pipecolic acidemia (links | edit)
- Methylmalonyl CoA epimerase (links | edit)
- Hypermethioninemia (links | edit)
- Cystathioninuria (links | edit)
- Vitamin B12 deficiency (links | edit)
- Hyperprolinemia (links | edit)
- Brunner syndrome (links | edit)
- Hypervalinemia (links | edit)
- Organic acidemia (links | edit)
- Vitamin B12 (links | edit)
- SUCLG1 (links | edit)
- Urocanic aciduria (links | edit)
- Carnosinemia (links | edit)
- Congenital disorders of amino acid metabolism (links | edit)
- Amino acid transport disorder (links | edit)
- Inborn errors of renal tubular transport (links | edit)
- Ocular albinism (links | edit)
- Tyrosinemia type III (links | edit)
- Multiple carboxylase deficiency (links | edit)
- Ethylene glycol poisoning (links | edit)
- Ocular albinism type 1 (links | edit)
- Hypertryptophanemia (links | edit)
- Molybdenum cofactor deficiency (links | edit)
- Iminoglycinuria (links | edit)
- Dopamine beta hydroxylase deficiency (links | edit)
- MMAA (links | edit)
- Tyrosinemia type II (links | edit)
- Haptocorrin (links | edit)
- List of causes of hypoglycemia (links | edit)
- Imerslund–Gräsbeck syndrome (links | edit)
- D-Glyceric acidemia (links | edit)
- Fanconi syndrome (links | edit)
- Argininemia (links | edit)
- ACSF3 (links | edit)
- Forensic Files season 3 (links | edit)
- List of disorders included in newborn screening programs (links | edit)
- Aminoacylase 1 deficiency (links | edit)
- William S. Sly (links | edit)
- Patricia Stallings (links | edit)
- Leon E. Rosenberg (links | edit)
- Tyrosinemia type I (links | edit)
- Branched-chain keto acid dehydrogenase kinase deficiency (links | edit)
- Combined malonic and methylmalonic aciduria (links | edit)
- Methylmalonic acidemia (transclusion) (links | edit)
- Talk:Methylmalonic acidemias (links | edit)
- Talk:Branched-chain amino acid (links | edit)
- Talk:Methylmalonic acidemia (transclusion) (links | edit)
- User:CopperKettle (links | edit)
- User:Madhero88/OthersBM (links | edit)
- User:Andrew Gray/med-stubs (links | edit)
- User:Rpinkham/sandbox (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia (links | edit)
- User:Drsalmanshah165/Books/Anaphylaxis (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-M (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-N (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-O (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-pha (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia0-pln (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-P (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-Q (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-R (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-S (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-T (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-U (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-V (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-W (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-X (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-Y (links | edit)
- User:Drsalmanshah165/Books/Medical Wikipedia 0-z (links | edit)
- User:Drsalmanshah165/Books/Medical wikipedia (links | edit)
- User:Drsalmanshah165/Books/Offline Medical Wikipedia (links | edit)
- User:Drsalmanshah165/Books/Offline Medical Wikipedia 0-Z (links | edit)
- User:MastCell/Ignored medical articles (links | edit)
- User:Umbacgra (links | edit)
- User:Daniel Mietchen/Wikidata lists/Items with Disease Ontology IDs (links | edit)
- User:Ricov53/sandbox (links | edit)
- User:Gavivz/Books/Inborn errors of metabolism (links | edit)
- User:Omer476/Books/Rare diseases (A-O) (links | edit)
- User:Gaurav Naik/sandbox (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- User:Canada Hky/NBS (links | edit)
- User:Y-S.Ko/Wikipedia course/Diseases (links | edit)
- User:Aherrera09/sandbox (links | edit)
- User:Sun Creator/A to An files (links | edit)
- User:Mmaguilar2/New Sandbox (links | edit)
- User talk:Anandks007/Med (links | edit)
- User talk:Pinar A. (links | edit)
- Wikipedia:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Wikipedia:WikiProject Medicine/Lists of pages/Low-importance medicine articles (links | edit)
- Wikipedia:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Wikipedia:WikiProject Medicine/Assessment/Articles to re-classify (links | edit)
- Wikipedia:WikiProject Short descriptions/wd/diseases (links | edit)
- Wikipedia:WikiProject Medicine/The ICD-11 coding challenge/900–999 (links | edit)
- Template:Amino acid metabolic pathology (links | edit)
- Template:Metabolic disorders of vitamins, coenzymes, and cofactors (links | edit)
- Category:Vitamin, coenzyme, and cofactor metabolism disorders (links | edit)
- Talk:Methylmalonic acidemias (transclusion) (links | edit)
