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Erythropoietic Porphyria
Erythropoietic porphyria
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Porphyrias
(9)
Porphyria
Acute intermittent porphyria
Hereditary coproporphyria
Erythropoietic protoporphyria
Variegate porphyria
Variegate porphyria
ALAD porphyria
Hepatoeryt- hropoietic porphyria
Hepatic porphyrias
Porphyria cutanea tarda
more...
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
Erythropoietic protoporphyria
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
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...
Medical terms
Diseases and disorders
Neuronopathy
Cystitis
Autosomal recessive disorders
Lucey-Driscoll syndrome
Rotor syndrome
Otospondyl- omegaepiphyseal dysplasia
Usher syndrome
Recessive multiple epiphyseal dysplasia
Dubin-Johnson syndrome
Congenital erythropoietic porphyria
Genetic disorder
Congenital erythropoietic porphyria
ALAD porphyria
Rotor syndrome
Recessive multiple epiphyseal dysplasia
Gastroenterology
Chronic lobular hepatitis
Cholestasis
Hemochromatosis
Porphyria
Dubin-Johnson syndrome
Syndromes
(9)
Cutis hyperelastica
Cushings syndrome
Ullrich-Turner syndrome
5p deletion syndrome
Crigler-najjar syndrome
Crigler-najjar syndrome
Lucey-Driscoll syndrome
Rotor syndrome
Usher syndrome
Dubin-Johnson syndrome
more...
Congenital disorders
Corpus callosum agenesis
Genetic disorders
Congenital
Congenital bilateral absence of vas deferens
Cutis hyperelastica
Tetrapyrroles
(38)
Conjugated bilirubin
Heme
Hydroxymethylbilane
Porphyrins
Protoporphyrin
Protoporphyrin
Protoporphyrin IX
Uroporphyrinogen III
Bilin (biochemistry)
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
Zinc protoporphyrin
more...
Biomolecules
Uroporphyrinogen
Enzyme
D-Aminolevulinic acid
Porphyrins
Heme
Metabolism
Heme metabolism intermediates
Porphobilinogen
Metabolic diseases
Porphyrins
Conjugated bilirubin
Enzyme
Skin conditions resulting from physical factors
Light sensitivity
Photodermatitis
Polymorphous light eruption
Solar urticaria
EC number
Uroporphyrinogen decarboxylase
PROTO oxidase
Porphobilinogen deaminase
Coproporphyrinogen oxidase
Uroporphyrinogen III synthase
ALA dehydratase
Ferrochelatase
Genetic disorders
(21)
Charcot-Marie-Tooth disease, type 4
X-linked sideroblastic anemia
Nonsyndromic deafness
Congenital erythropoietic porphyria
Porphyria
Porphyria
Cutis hyperelastica
Acute intermittent porphyria
Hereditary coproporphyria
Erythropoietic protoporphyria
Variegate porphyria
ALAD porphyria
Porphyria cutanea tarda
Lucey-Driscoll syndrome
Rotor syndrome
Ullrich-Turner syndrome
5p deletion syndrome
Crigler-najjar syndrome
Otospondyl- omegaepiphyseal dysplasia
Usher syndrome
Recessive multiple epiphyseal dysplasia
Dubin-Johnson syndrome
more...
Diseases and disorders
(44)
Porphyria congenital erythropoietic
Salaam seizures
Mycobacterial
Protoporphyria
Hereditary hyperbilirubinemia
Hereditary hyperbilirubinemia
Photosensitive epilepsy
Polyglucosan body disease adult
Protoporphyria erythropoietic
Porphyria hereditary coproporphyria
Coccidioidomycosis
Ehlers-danlos syndrome dermatosparaxis type
Lymphohistiocytosis
Cytomegalovirus
Silicosis
Chemical pneumonitis
Primary hyperoxaluria
Congenital erythropoietic porphyria
Porphyria
Cutis hyperelastica
Conns Syndrome
Acute intermittent porphyria
Corpus callosum agenesis
Hereditary coproporphyria
Variegate porphyria
Cushings syndrome
Hepatoeryt- hropoietic porphyria
Porphyrias
Porphyria cutanea tarda
Lucey-Driscoll syndrome
Chronic cold urticaria
Rotor syndrome
Chronic lobular hepatitis
Charcot-Marie-Tooth disease, type 4
X-linked sideroblastic anemia
5p deletion syndrome
Cholestasis
Usher syndrome
Photodermatitis
Polymorphous light eruption
Hemochromatosis
Hydrops fetalis
Metabolic diseases
Cystitis
Urticarial
more...
See also
(20)
Conns Syndrome
Erythropoietic
Uroporphyrinogen III synthase
Heme arginate
Porphyrin metabolism
Porphyrin metabolism
Chronic cold urticaria
ALA dehydratase
Hematin
ALA synthase
Cutaneous porphyria
PPOX
Porphyric
Cryptogenic fibrosing alveolitis
Panhematin
Ferrochelatase
Uroporphyrinogen I
Porfiria
Autosomal dominant
Autosomal recessive
Cytosol
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