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
24 clinical trials for this condition and its sub-types, 0 tagged with Inherited porphyria itself.
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Sub-types of Inherited porphyria
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Erythropoietic protoporphyria 15 trials
2 sub-types
- X-linked erythropoietic protoporphyria 10 trials
- Autosomal erythropoietic protoporphyria 0 trials · 3 incl. sub-types Sub-types →
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CPOX-related hereditary coproporphyria 0 trials · 5 incl. sub-types
2 sub-types
- Hereditary coproporphyria 5 trials
- Harderoporphyria 0 trials
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HMBS-related hepatic porphyria 0 trials · 5 incl. sub-types
4 sub-types
- Acute intermittent porphyria 5 trials
- Encephalopathy, porphyria-related 0 trials
- Leukoencephalopathy, porphyria-related 0 trials
- Porphyria, acute intermittent, nonerythroid variant 0 trials
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Cutaneous porphyria 2 trials
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PPOX-related hepatic porphyria 0 trials · 2 incl. sub-types
1 sub-type
- Variegate porphyria 2 trials Sub-types →
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UROD-related inherited porphyria 0 trials · 1 incl. sub-types
2 sub-types
- Familial porphyria cutanea tarda 1 trial
- Hepatoerythropoietic porphyria 0 trials
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Chester porphyria 0 trials
Most studied deeper sub-types
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