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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
C C- C1 C3 C5 C6 C7 CA CB CC CD CE CF CG CH CI CJ CK CL CM CN CO CP CQ CR CS CT CU CV CW CX CY CZ
CO COA COB COC COD COE COF COG COH COI COK COL COM CON COO COP COQ COR COS COT COU COV COW COX COY COZ

congenital hepatic porphyria

[disorders characterized by the liver excessively producing porphyrins or their precursors, arising from abnormalities in the regulation of the porphyrin-heme pathway existing at, and usually before, birth regardless of causation; porphyria, acute intermittent and porphyria cutanea tarda are types of hepatic porphyria. ( CSP )]
UMLS (CSP) C0687708
 
Disease or Syndrome
Relation/PAR: Hepatic Disorder
DIS PORPHYRIN METABOLISM
congenital disorder
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