Inherited porphyria
MONDO:0019142Porphyrias constitute a group of eight hereditary metabolic diseases characterized by intermittent neuro-visceral manifestations, cutaneous lesions or by the combination of both.
Also known as: disorder of porphyrin and heme metabolism, disorder of porphyrin metabolism, porphyria, hereditary porphyria, Hematoporphyria, Porphyrinopathy
51 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Erythropoietic protoporphyria
(13)
X-linked erythropoietic protoporphyria
(9)
Hereditary coproporphyria
(5)
Acute intermittent porphyria
(4)
Cutaneous porphyria
(2)
Protoporphyria, erythropoietic, 1
(2)
Variegate porphyria
(2)
Autosomal erythropoietic protoporphyria
(0)
Chester porphyria
(0)
CPOX-related hereditary coproporphyria
(0)
Encephalopathy, porphyria-related
(0)
Erythropoietic uroporphyria associated with myeloid malignancy
(0)
Familial porphyria cutanea tarda
(0)
Harderoporphyria
(0)
Hepatoerythropoietic porphyria
(0)
HMBS-related hepatic porphyria
(0)
Leukoencephalopathy, porphyria-related
(0)
Porphyria, acute intermittent, nonerythroid variant
(0)
Porphyria due to ALA dehydratase deficiency
(0)
PPOX-related hepatic porphyria
(0)