Carbamoylphosphate synthetase deficiency (Q40018): Difference between revisions
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A deficiência de carbamoilfosfato sintetase é um distúrbio do ciclo da ureia estritamente limitado ao fígado e ao intestino, que resulta em hiperamonemia congênita e síntese defeituosa de citrulina. | |||
| description / en | description / en | ||
Carbamyl phosphate synthetase deficiency is an urea cycle disorder strictly limited to the liver and intestine that results in congenital hyperammonemia and defective citrulline synthesis. | |||
Revision as of 05:39, 13 August 2026
Carbamyl phosphate synthetase deficiency is an urea cycle disorder strictly limited to the liver and intestine that results in congenital hyperammonemia and defective citrulline synthesis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 5C50.A1 |
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| English | Carbamoylphosphate synthetase deficiency |
Carbamyl phosphate synthetase deficiency is an urea cycle disorder strictly limited to the liver and intestine that results in congenital hyperammonemia and defective citrulline synthesis. |
