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Variegate Porphyria
Variegate porphyria
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Porphyrias
(9)
Porphyria
Hereditary coproporphyria
Erythropoietic porphyrias
ALA dehydratase deficiency
Hepatic porphyrias
Hepatic porphyrias
Hepatoeryt- hropoietic porphyria
Porphyria cutanea tarda
Porphyria, acute intermittent
Erythropoietic protoporphyria
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Skin conditions resulting from errors in metabolism
(86)
Congenital erythropoietic porphyria
Pseudoporphyria
Adrenoleuk- odystrophy
Alkaptonuria
Amyloid purpura
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 porphyrias
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
Porphyria, acute intermittent
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
Verruciform xanthoma
Waxy skin
Xanthelasma
Xanthoma
Xanthoma diabeticorum
Xanthoma planum
Xanthoma striatum palmare
Xanthoma tendinosum
Xanthoma tuberosum
Xanthomatosis
Xanthomatous biliary cirrhosis
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Genetic disorders
(20)
Lucey-Driscoll syndrome
Rotor syndrome
Spondyloep- imetaphyseal dysplasia, Strudwick type
Lentiginosis
Very long-chain acyl coenzyme A dehydrogenase deficiency
Very long-chain acyl coenzyme A dehydrogenase deficiency
Crigler-najjar syndrome
Progeria
Dubin-Johnson syndrome
Pseudoxanthoma elasticum
Peutz-jeghers syndrome
Partial trisomy
22q11.2 deletion syndrome
Hereditary disorder
Porphyria
Hereditary coproporphyria
ALA dehydratase deficiency
Congenital erythropoietic porphyria
Porphyria cutanea tarda
Porphyria, acute intermittent
Erythropoietic protoporphyria
more...
Diseases and disorders
(28)
Chronic cold urticaria
Polyglucosan body disease adult
Porphyria congenital erythropoietic
Hereditary hyperbilirubinemia
Porphyria hereditary coproporphyria
Porphyria hereditary coproporphyria
Protoporphyria
Hemochromatosis
Angioedema
Urticarial
Metabolic disorders
FTLD
Alzheimer disease
Pemphigus vulgaris
Porphyria
Hereditary coproporphyria
Porphyrias
Congenital erythropoietic porphyria
Hepatoeryt- hropoietic porphyria
Porphyria cutanea tarda
Porphyria, acute intermittent
Lucey-Driscoll syndrome
Rotor syndrome
Spondyloep- imetaphyseal dysplasia, Strudwick type
Lentiginosis
Progeria
Pseudoxanthoma elasticum
Partial trisomy
22q11.2 deletion syndrome
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Gastroenterology
Acute pancreatitis
Porphyria
Hemochromatosis
Dubin-Johnson syndrome
Angioedema
Peutz-jeghers syndrome
Tetrapyrroles
(38)
Heme
Hydroxymethyl bilane
Porphyrin
Protoporphyrin IX
Uroporphyrinogen III
Uroporphyrinogen III
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
Protoporphyrin
Talaporfin
Temoporfin
Tetraphenylporphine sulfonate
Tetrapheny- lporphyrin
Tetrapyrrole
Urobilin
Urobilinogen
Zinc protoporphyrin
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Biomolecules
Uroporphyrinogen
D-Aminolevulinic acid
Porphyrin
Heme
Metabolism
Heme metabolism intermediates
Porphobilinogen
Porphyrin
Metabolic disorders
Nitrogen heterocycles
Pyrrole
Pyrroline
Porphyrin
Urticaria and angioedema
(33)
Solar urticaria
Acquired C1 esterase inhibitor deficiency
Acute urticaria
Adrenergic urticaria
Anaphylaxis
Anaphylaxis
Angioedema
Aquagenic urticaria
Capillary leak syndrome
Cholinergic urticaria
Chronic cold urticaria
Chronic urticaria
Contact dermatitis
Dermatographic urticaria
Drug-induced urticaria
Exercise urticaria
Familial cold urticaria
Galvanic urticaria
Gleich's syndrome
Heat urticaria
Hereditary angioedema
Localized heat contact urticaria
Physical urticaria
Pressure urticaria
Primary cold contact urticaria
Reflex cold urticaria
Schnitzler syndrome
Secondary cold contact urticaria
Urticaria-like follicular mucinosis
Urticarial
Urticarial allergic eruption
Urticarial dermatoses
Urticarial syndromes
Vibratory angioedema
more...
EC number
PROTO oxidase
Uroporphyrinogen decarboxylase
Porphobilinogen deaminase
ALA dehydratase
Coproporphyrinogen oxidase
Ferrochelatase
See also
(20)
Heme arginate
PPOX
Common Professional Exam
ALA synthase
Admissions essay
Admissions essay
College admission
Bluebeard by Kurt Vonnegut
Porphyrin metabolism
Critical care unit
Cutaneous porphyria
Porphyric
University of California Press
Literary devices
Photosensitivity
Literary naturalism
Erythropoietic
Key Club International
Hematin
Protoporphyrinogen IX
The International League of Dermatological Societies
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