Ornithine carbamoyl phosphate deficiency

Introduction: Ornithine carbamoyl phosphate deficiency

Description of Ornithine carbamoyl phosphate deficiency

Ornithine carbamoyl phosphate deficiency: inherited urea cycle disorder associated with deficiency of the enzyme ornithine carbamoyltransferase, transmitted as a sex-linked trait and featuring elevations of amino acids and ammonia in the serum.
Source: CRISP

Ornithine carbamoyl phosphate deficiency: Related Topics

These medical condition or symptom topics may be relevant to medical information for Ornithine carbamoyl phosphate deficiency:

• Carbamoyl phosphate
• Ornithine
• Phosphate
• Deficiency

Terms associated with Ornithine carbamoyl phosphate deficiency:

Broader terms for Ornithine carbamoyl phosphate deficiency

• enzyme deficiency
• inborn urea cycle disorder

Source - CRISP

The term Ornithine carbamoyl phosphate deficiency can be used for:

• congenital hyperammonemia type II
• ornithine carbamoyltransferase deficiency
• ornithine transcarbamylase deficiency

Source: CRISP

Other terms that may be related to Ornithine carbamoyl phosphate deficiency:

• ornithine carbamoyltransferase

Source: CRISP

The description of Ornithine carbamoyl phosphate deficiency may also be used for the following terms:

• OCP deficiency

Source: CRISP

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Neuroleptic

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