Urea cycle disorder | Deficient enzymes | Inheritance pattern |
Hyperammonemia Type 1 | Carbamoyl phosphate synthase 1 | Autosomal Recessive |
Hyperammonemia Type 2 | Ornithine trans carbamylase | X-linked Recessive |
HHH Syndrome | Ornithine transporter | Autosomal Recessive |
Orotic acid aciduria Type 2 | Orotidylic acid decarboxylase | Autosomal Recessive |
Citrullinemia Type 1 | Argininosuccinate Synthetase | Autosomal Recessive |

