disease caused by disruption of disease has basis in disruption of porphyrin-containing compound metabolic process inborn disorder of porphyrin metabolism An acquired metabolic disease that is has its basis in the disruption of porphyrin-containing compound metabolic process. Editor note: we follow ORDO and treat this as inborn. However, some form of porphyria (e.g PCT) may be acquired. ICD10:E80.0 ICD10:E80.1 ICD10:E80.2 ICD10:E80.3 ICD10:E80.4 ICD10:E80.5 ICD10:E80.6 ICD10:E80.7 MONDO:0017754 Orphanet:309813 SCTID:403832004 UMLS:C1275125 disorder of porphyrin and haem metabolism inborn disorder of porphyrin and haem metabolism inborn error of porphyrin-containing compound metabolic process inborn porphyrin-containing compound metabolic process disorder inherited disorder of porphyrin metabolism rare inborn error of porphyrin-containing compound metabolic process inborn errors of metabolism porphyrin metabolism disease