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Urea Cycle Disorders, Inborn

Categorical breakdown of terms falling inder the category of Urea Cycle Disorders, Inborn. Sub categories will become more specific in nature to the terms listed for Urea Cycle Disorders, Inborn.

Sub-Categories

Terms

Argininosuccinic Aciduria - Rare autosomal recessive disorder of the urea cycle which leads to the accumulation of argininosucci...

Carbamoyl-Phosphate Synthase I Deficiency Disease - A urea cycle disorder manifesting in infancy as lethargy, emesis, seizures, alterations of muscle to...

Citrullinemia - A group of diseases related to a deficiency of the enzyme ARGININOSUCCINATE SYNTHASE which causes an...

Hyperargininemia - A rare autosomal recessive disorder of the urea cycle. It is caused by a deficiency of the hepatic e...

Ornithine Carbamoyltransferase Deficiency Disease - An inherited urea cycle disorder associated with deficiency of the enzyme ORNITHINE CARBAMOYLTRANSFE...

Urea Cycle Disorders, Inborn - Rare congenital metabolism disorders of the urea cycle. The disorders are due to mutations that resu...