Pages that link to "Maple syrup urine disease"
Showing 140 items.
- Phenylketonuria (links | edit)
- Thiamine (links | edit)
- Human genome (links | edit)
- List of genetic disorders (links | edit)
- Isoleucine (links | edit)
- Leucine (links | edit)
- Valine (links | edit)
- Neonatal heel prick (links | edit)
- Alkaptonuria (links | edit)
- Founder effect (links | edit)
- Methylmalonic acidemias (links | edit)
- Propionic acidemia (links | edit)
- Hyperammonemia (links | edit)
- Urinalysis (links | edit)
- Waardenburg syndrome (links | edit)
- Homocystinuria (links | edit)
- Newborn screening (links | edit)
- Cystinuria (links | edit)
- Ornithine transcarbamylase deficiency (links | edit)
- Inborn errors of metabolism (links | edit)
- Opisthotonus (links | edit)
- Ketotic hypoglycemia (links | edit)
- Trimethylaminuria (links | edit)
- Sotolon (links | edit)
- Isovaleric acidemia (links | edit)
- Maple syrup urine disease (transclusion) (links | edit)
- Maple Syrup Urine Disease (redirect page) (links | edit)
- Cystinosis (links | edit)
- Citrullinemia (links | edit)
- Beta-ketothiolase deficiency (links | edit)
- 3-Hydroxy-3-methylglutaryl-CoA lyase deficiency (links | edit)
- Tyrosinemia (links | edit)
- Hartnup disease (links | edit)
- Dentate nucleus (links | edit)
- Glutaric aciduria type 1 (links | edit)
- Saccharopinuria (links | edit)
- Ochronosis (links | edit)
- Lysinuric protein intolerance (links | edit)
- Maple-syrup-urine disease (redirect page) (links | edit)
- Maple syrup urinedisease (redirect page) (links | edit)
- MSUD (redirect page) (links | edit)
- Hyperlysinemia (links | edit)
- Branched-chain amino acid (links | edit)
- Branched-chain alpha-keto acid dehydrogenase complex (links | edit)
- Chromosome 1 (links | edit)
- Chromosome 6 (links | edit)
- Chromosome 7 (links | edit)
- Tetrahydrobiopterin deficiency (links | edit)
- Chromosome 19 (links | edit)
- Hermansky–Pudlak syndrome (links | edit)
- Medical genetics (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)
- 3-Methylglutaconic aciduria (links | edit)
- 6-Pyruvoyltetrahydropterin synthase deficiency (links | edit)
- 3-Methylcrotonyl-CoA carboxylase deficiency (links | edit)
- Methylmalonyl-CoA mutase deficiency (links | edit)
- Urine (links | edit)
- Glycine encephalopathy (links | edit)
- Clinic for Special Children (links | edit)
- Hawkinsinuria (links | edit)
- Fumarase deficiency (links | edit)
- Maple Syrup Urine Disorder (redirect page) (links | edit)
- Newborn screening (links | edit)
- Leucinosis (redirect page) (links | edit)
- List of diseases (L) (links | edit)
- User:Davidruben/OrphaNet (links | edit)
- User talk:Solon.KR (links | edit)
- User talk:Anandks007/Med (links | edit)
- Aminoaciduria (links | edit)
- List of MeSH codes (C18) (links | edit)
- List of MeSH codes (C16) (links | edit)
- List of MeSH codes (C10) (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)
- Isobutyryl-coenzyme A dehydrogenase deficiency (links | edit)
- Robert Guthrie (links | edit)
- Carbamoyl phosphate synthetase I deficiency (links | edit)
- Ethylmalonic encephalopathy (links | edit)
- Sarcosinemia (links | edit)
- Ornithine translocase deficiency (links | edit)
- Prolidase deficiency (links | edit)
- Pipecolic acidemia (links | edit)
- Hypermethioninemia (links | edit)
- Cystathioninuria (links | edit)
- Hyperprolinemia (links | edit)
- Ketoacidemia (redirect page) (links | edit)
- Brunner syndrome (links | edit)
- Hypervalinemia (links | edit)
- Organic acidemia (links | edit)
- Branched-chain ketoaciduria (redirect page) (links | edit)
- BCKDHA (links | edit)
- DBT (gene) (links | edit)
- BCKDHB (links | edit)
- BCKDK (links | edit)
- Maple sugar urine disease (redirect page) (links | edit)
- Urocanic aciduria (links | edit)
- Maple Syrup Urine Syndrome (redirect page) (links | edit)
- List of medical abbreviations: M (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)
- Α-Ketoisocaproic acid (links | edit)
- List of skin conditions (links | edit)
- Ocular albinism (links | edit)
- Tyrosinemia type III (links | edit)
- Msud (redirect page) (links | edit)
- Amish (links | edit)
- Ocular albinism type 1 (links | edit)
- Hypertryptophanemia (links | edit)
- Iminoglycinuria (links | edit)
- Dopamine beta hydroxylase deficiency (links | edit)
- Tyrosinemia type II (links | edit)
- List of Mystery Diagnosis episodes (links | edit)
- Medical genetics of Jews (links | edit)
- Global developmental delay (links | edit)
- List of causes of hypoglycemia (links | edit)
- D-Glyceric acidemia (links | edit)
- Fanconi syndrome (links | edit)
- Argininemia (links | edit)
- List of disorders included in newborn screening programs (links | edit)
- Aminoacylase 1 deficiency (links | edit)
- Maple syrup urine syndrome (redirect page) (links | edit)
- Nagwa Abdel Meguid (links | edit)
- Reidenbach Old Order Mennonites (links | edit)
- John Menkes (links | edit)
- Health among the Amish (links | edit)
- L. Emmett Holt Jr. (links | edit)
- Maple syrup urine (redirect page) (links | edit)
- Robert Guthrie (links | edit)
- Joseph Dancis (links | edit)
- Tyrosinemia type I (links | edit)
- Gerry Downes (links | edit)
- Relief Therapeutics (links | edit)
- Smell as evidence of disease (links | edit)
- Branched-chain keto acid dehydrogenase kinase deficiency (links | edit)
- Alloisoleucine (links | edit)
- Methylmalonic acidemia with homocystinuria (links | edit)