Prev Term: ornithine aminotransferase deficiency
Next Term: ornithine carbamoyltransferase
ornithine carbamoyl phosphate deficiency
Used for:
congenital hyperammonemia type II
Used for:
ornithine carbamoyltransferase deficiency
Used for:
ornithine transcarbamylase deficiency
See for:
OCP deficiency
Broader Terms:
enzyme deficiency
Broader Terms:
inborn urea cycle disorder
Related Terms:
ornithine carbamoyltransferase
Scope Note:
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.
Term Number:
1849-9662
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