disease has basis in disruption of disease caused by disruption of porphyrin-containing compound metabolic process inborn disorder of porphyrin metabolism https://www.malacards.org/card/porphyria inborn disorder of porphyrin and haem metabolism disorder of porphyrin and haem metabolism Orphanet:309813 An inherited metabolic disease that is has its basis in the disruption of porphyrin-containing compound metabolic process. SCTID:403832004 rare inborn error 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. inborn porphyrin-containing compound metabolic process disorder MONDO:0017754 GARD:0021346 inborn error of porphyrin-containing compound metabolic process inherited disorder of porphyrin metabolism inborn errors of metabolism porphyrin metabolism disease