UMLS. CSP-HL7-ICD9CM-NCI-NDFRT-RXNORM
%
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
O O- O0 O1 O2 O3 OA OB OC OD OE OF OG OH OI OJ OK OL OM ON OO OP OR OS OT OU OV OW OX OY OZ
OCA OCB OCC OCD OCE OCH OCK OCL OCP OCT OCU

OCP 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. ( CSP )]
UMLS (CSP) C0597143
 
Disease or Syndrome
Relation/PAR: enzyme deficiency
inborn urea cycle disorder

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