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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
H H+ H1 HA HB HC HD HE HF HG HH HI HK HL HM HN HO HP HQ HR HS HT HU HV HX HY HZ
HYA HYB HYC HYD HYG HYH HYK HYM HYO HYP HYS HYT

hyperornithinemia

[excess of ornithine in the plasma, such as occurs in the genetic disorders gyrate atrophy of choroid and retina and hyperornithinemia-hyperamonemia-homocitrullinuria syndrome. ( CSP )]
UMLS (CSP) C0599035
 
Disease or Syndrome
Relation/PAR: Amino Acid Metabolism, Inborn Errors
Degeneration of retina
enzyme deficiency

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