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 |