Porphyrin metabolism disease
MONDO:0037821A disease that has its basis in the disruption of porphyrin-containing compound metabolic process.
Also known as: disorder of porphyrin metabolism, disorder of porphyrin-containing compound metabolic process, porphyrin-containing compound metabolic process disease, disorder of porphyrin and heme metabolism
66 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)
Porphyria
(8)
Hereditary coproporphyria
(5)
Acute intermittent porphyria
(4)
Hepatic 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)