The following pages link to Alkaptonuria
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Glycine encephalopathy (links | edit)
- Homogentisic acid (links | edit)
- 4-Hydroxyphenylpyruvate dioxygenase (links | edit)
- Hawkinsinuria (links | edit)
- Fumarase deficiency (links | edit)
- Aminoaciduria (links | edit)
- List of MeSH codes (C18) (links | edit)
- List of MeSH codes (C16) (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)
- Black Urine Disease (redirect page) (links | edit)
- Hyperhomocysteinemia (links | edit)
- Black urine disease (redirect page) (links | edit)
- Alkaptonuric ochronosis (redirect page) (links | edit)
- Isobutyryl-coenzyme A dehydrogenase deficiency (links | edit)
- Carbamoyl phosphate synthetase I deficiency (links | edit)
- Ethylmalonic encephalopathy (links | edit)
- Sarcosinemia (links | edit)
- Nitisinone (links | edit)
- Ornithine translocase deficiency (links | edit)
- Prolidase deficiency (links | edit)
- Alcaptonurea (redirect page) (links | edit)
- Pipecolic acidemia (links | edit)
- Homogentisate 1,2-dioxygenase (links | edit)
- Hypermethioninemia (links | edit)
- Cystathioninuria (links | edit)
- Mendelian traits in humans (links | edit)
- Hyperprolinemia (links | edit)
- Brunner syndrome (links | edit)
- Maleylacetoacetate isomerase (links | edit)
- Hypervalinemia (links | edit)
- Organic acidemia (links | edit)
- GSTZ1 (links | edit)
- Dioxygenase (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)
- List of skin conditions (links | edit)
- Ocular albinism (links | edit)
- Tyrosinemia type III (links | edit)
- William A. Gahl (links | edit)
- Allelic heterogeneity (links | edit)
- Ocular albinism type 1 (links | edit)
- Hypertryptophanemia (links | edit)
- Iminoglycinuria (links | edit)