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Erythropoietic Protoporphyria
Erythropoietic protoporphyria
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Porphyrias
(9)
Porphyria
Acute intermittent porphyria
Hereditary coproporphyria
Variegate porphyria
ALA dehydratase deficiency
ALA dehydratase deficiency
Porphyria, erythropoietic
Hepatic porphyrias
Hepatoeryt- hropoietic porphyria
Porphyria cutanea tarda
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Skin conditions resulting from errors in metabolism
(86)
Congenital erythropoietic porphyria
Pseudoporphyria
Acute intermittent porphyria
Adrenoleuk- odystrophy
Alkaptonuria
Alkaptonuria
Amyloid purpura
Amyloidosis
Apolipoprotein B deficiency
B-mannosidase deficiency
CADASIL syndrome
Calcinosis cutis
Carotenosis
Cerebrotendineous xanthomatosis
Citrullinemia
Combined hyperlipidemia
Diabetic bulla
Diabetic cheiroarthropathy
Diabetic dermadrome
Diabetic dermopathy
Dystrophic calcinosis cutis
Eruptive xanthoma
Fabry disease
Familial apoprotein CII deficiency
Familial dysbetalip- oproteinemia
Familial hypertrigl- yceridemia
Farber disease
Fucosidosis
Gaucher's disease
Gout
Hartnup disease
Hepatoeryt- hropoietic porphyria
Hereditary coproporphyria
Heredofamilial amyloidosis
Hunter syndrome
Hurler syndrome
Hyaluronidase deficiency
Iatrogenic calcinosis cutis
Idiopathic scrotal calcinosis
Lafora disease
Lesch–Nyhan syndrome
Lichen amyloidosis
Limited joint mobility
Lipoprotein lipase deficiency
Macular amyloidosis
Medication-induced hyperlipop- roteinemia
Metastatic calcinosis cutis
Morquio syndrome
Myxedema
Necrobiosis lipoidica
Niemann–Pick disease
Nodular amyloidosis
Nodular xanthoma
Normolipop- roteinemic xanthomatosis
Ochronosis
Osteoma cutis
Palmar xanthoma
Phenylketonuria
Porphyria
Porphyria cutanea tarda
Porphyria, erythropoietic
Primary cutaneous amyloidosis
Primary systemic amyloidosis
Prolidase deficiency
Secondary cutaneous amyloidosis
Secondary systemic amyloidosis
Sialidosis
Sitosterolemia
Subepidermal calcified nodule
Tangier disease
Transient erythroporphyria of infancy
Traumatic calcinosis cutis
Tuberoeruptive xanthoma
Tumoral calcinosis
Urbach–Wiethe disease
Variegate porphyria
Verruciform xanthoma
Waxy skin
Xanthelasma
Xanthoma
Xanthoma diabeticorum
Xanthoma planum
Xanthoma striatum palmare
Xanthoma tendinosum
Xanthoma tuberosum
Xanthomatosis
Xanthomatous biliary cirrhosis
more...
Genetic disorders
(16)
Lucey-Driscoll syndrome
Emery-Dreifuss Syndrome
Rotor syndrome
X-linked sideroblastic anemia
Otospondyl- omegaepiphyseal dysplasia
Otospondyl- omegaepiphyseal dysplasia
Crigler-najjar syndrome
Recessive multiple epiphyseal dysplasia
Familial mediterranean fever
Elliptocytosis, hereditary
Porphyria
Acute intermittent porphyria
Hereditary coproporphyria
Congenital erythropoietic porphyria
Variegate porphyria
ALA dehydratase deficiency
Porphyria cutanea tarda
more...
Hematology
E-rosetting
Factor V Leiden thrombophilia
Erythrocyte
Hereditary hemochromatosis
Porphyria
Gastroenterology
Cholestasis
Porphyria
Familial mediterranean fever
Hereditary hemochromatosis
Integumentary system
Erythema toxicum
Photodermatosis
Actinic prurigo
Hydroa vacciniforme
Chronic urticaria
Erythema multiforme
Pseudoporphyria
Tetrapyrroles
(38)
Heme
Hydroxymethyl bilane
Porphyrins
Protoporphyrin
Protoporphyrin IX
Protoporphyrin IX
Bilin (biochemistry)
Bilirubin
Bilirubin (data page)
Biliverdin
Chlorophyll
Chlorophyll a
Chlorophyll b
Chlorophyll c1
Chlorophyll c2
Chlorophyll d
Chlorophyllin
Coproporphyrinogen III
Corrin
Corrole
Heme C
Heme a
Heme b
Heme o
Phycobilin
Phycocyanobilin
Phycoerythrobilin
Phycoerythrocyanin
Phycourobilin
Porphin
Talaporfin
Temoporfin
Tetraphenylporphine sulfonate
Tetrapheny- lporphyrin
Tetrapyrrole
Urobilin
Urobilinogen
Uroporphyrinogen III
Zinc protoporphyrin
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Metabolism
Heme metabolism intermediates
Porphobilinogen
Inborn error of metabolism
Porphyrins
Skin conditions resulting from physical factors
Polymorphous light eruption
Solar urticaria
Light sensitivity
Photodermatitis
Photodermatosis
Actinic prurigo
Hydroa vacciniforme
Medicine
Diseases and disorders
Heme arginate
Photoprotection
Archives of Dermatology
Hepatic porphyrias
EC number
PROTO oxidase
Uroporphyrinogen decarboxylase
Ferrochelatase
Coproporphyrinogen oxidase
ALA dehydratase
Porphobilinogen deaminase
Diseases and disorders
(37)
Esophageal atresia
Protoporphyria
Eosinophilic granuloma
Porphyria congenital erythropoietic
Photosensitive epilepsy
Photosensitive epilepsy
Hereditary hyperbilirubinemia
Ependymoma
Porphyria hereditary coproporphyria
Early constraint defects
Ehlers-danlos syndrome dermatosparaxis type
Progressive multifocal leukoencephalopathy
Encephalotrigeminal Angiomatosis
Actinic keratosis
Erythremia
Tinea versicolor
Porphyria
Acute intermittent porphyria
Hereditary coproporphyria
Congenital erythropoietic porphyria
Variegate porphyria
Porphyrias
Hepatoeryt- hropoietic porphyria
Porphyria cutanea tarda
Polymorphous light eruption
Chronic cold urticaria
Lucey-Driscoll syndrome
Rotor syndrome
X-linked sideroblastic anemia
Factor V Leiden thrombophilia
Photodermatitis
Familial mediterranean fever
Hydroa vacciniforme
Hereditary hemochromatosis
Inborn error of metabolism
Erythema multiforme
Elliptocytosis, hereditary
Cholestasis
more...
See also
(20)
epidermolysis bullosa letalis
Extradural hematoma
Epiphysiodesis
Epikeratophakia
Erythroplasia of Queyrat
Erythroplasia of Queyrat
Plantar reflex
Eyelid drooping
Enterobius vermicularis
Erythropoietic
Chronic cold urticaria
Afamelanotide
Porphyrin metabolism
Alad
PPOX
Cutaneous porphyria
ALA synthase
Methoxsalen
Hematin
Uroporphyrinogen
The International League of Dermatological Societies
more...
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