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
64 clinical trials for this condition and its sub-types, 0 tagged with Porphyrin metabolism disease itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Part of
Sub-types of Porphyrin metabolism disease
-
Inborn disorder of porphyrin metabolism 0 trials · 63 incl. sub-types
4 sub-types
- Inborn disorder of bilirubin metabolism 0 trials · 39 incl. sub-types Sub-types →
- Inherited porphyria 0 trials · 24 incl. sub-types Sub-types →
- X-linked sideroblastic anemia 1 0 trials
- Heme oxygenase 1 deficiency 0 trials
-
Porphyria 8 trials · 25 incl. sub-types
3 sub-types
- Inherited porphyria 0 trials · 24 incl. sub-types Sub-types →
- Hepatic porphyria 4 trials · 23 incl. sub-types Sub-types →
- Acquired porphyria 0 trials Sub-types →
Most studied deeper sub-types
Transient familial neonatal hyperbilirubinemia
(18)
Progressive familial intrahepatic cholestasis
(16)
Erythropoietic protoporphyria
(15)
X-linked erythropoietic protoporphyria
(10)
Acute intermittent porphyria
(5)
Hereditary coproporphyria
(5)
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)
Arthrogryposis-renal dysfunction-cholestasis syndrome
(1)
Cholestasis, progressive familial intrahepatic, 5
(1)
Cholestasis, progressive familial intrahepatic, 6
(1)
Familial porphyria cutanea tarda
(1)
Hereditary North American Indian childhood cirrhosis
(1)
We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.