Inborn disorder of porphyrin metabolism
MONDO:0017754An inherited metabolic disease that is has its basis in the disruption of porphyrin-containing compound metabolic process.
Also known as: 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
79 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Transient familial neonatal hyperbilirubinemia
(16)
Progressive familial intrahepatic cholestasis
(15)
Erythropoietic protoporphyria
(13)
X-linked erythropoietic protoporphyria
(9)
Hereditary coproporphyria
(5)
Acute intermittent porphyria
(4)
Progressive familial intrahepatic cholestasis type 1
(4)
Progressive familial intrahepatic cholestasis type 2
(4)
Bilirubin encephalopathy
(3)
Benign recurrent intrahepatic cholestasis
(2)
Cholestasis, progressive familial intrahepatic, 4
(2)
Cutaneous porphyria
(2)
Progressive familial intrahepatic cholestasis type 3
(2)
Protoporphyria, erythropoietic, 1
(2)
Variegate porphyria
(2)
Cholestasis, progressive familial intrahepatic, 5
(1)
Cholestasis, progressive familial intrahepatic, 6
(1)
Hereditary North American Indian childhood cirrhosis
(1)
Arthrogryposis, renal dysfunction, and cholestasis 1
(0)
Arthrogryposis, renal dysfunction, and cholestasis 2
(0)