DIS PORPHYRIN METABOLISM
[group of disorders characterized by the excessive production of porphyrins or their precursors that arises from abnormalities in the regulation of the porphyrin-heme pathway; acquired porphyrias, which are due to inhibition of enzymes in the metabolic pathway by a drug, toxin or abnormal metabolite, are more common than those which are inherited. ( CSP )]
UMLS (ICD9CM) C0032708- Disease or Syndrome
Relation/PAR: Metabolic Disease
Congenital Metabolic Disorder
Skin Diseases, Metabolic
Congenital Metabolic Disorder
Skin Diseases, Metabolic
Relation/CHD: congenital erythropoietic porphyria
EPP (erythropoietic protoporphyria porphyria)
congenital hepatic porphyria
congenital erythropoietic porphyria
Porphyria, Hepatic
Porphyria, Erythrohepatic
EPP (erythropoietic protoporphyria porphyria)
congenital hepatic porphyria
congenital erythropoietic porphyria
Porphyria, Hepatic
Porphyria, Erythrohepatic
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