Coproporphyria
Digestive system hereditary disorder
Hepatic porphyria
Hereditary metabolic disease
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Hereditary coproporphyria (disorder)
Hereditary coproporphyria
HCP - Hereditary coproporphyria
Coproporphyrinogen oxidase deficiency
Berger-Goldberg syndrome
CPO deficiency
CPO - Coproporphyrinogen oxidase deficiency
Porphyria hepatica II
CPRO deficiency
hereditaire coproporfyrie
Id7425008
StatusDefined
Finding siteLiver structure
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetE80.2
RuleTRUE
AdviceALWAYS E80.2
CorrelationSNOMED CT source code to target map code correlation not specified
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Erythropoietic coproporphyria
Homozygous hereditary coproporphyria