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Gunther Disease
Gunther disease
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Skin conditions resulting from errors in metabolism
(86)
Acute intermittent porphyria
Erythropoietic porphyria
Erythropoietic protoporphyria
Hepatoeryt- hropoietic porphyria
Hereditary coproporphyria
Hereditary coproporphyria
Neuraminidase deficiency
Porphyria
Porphyria cutanea tarda
Variegate porphyria
Adrenoleuk- odystrophy
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
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
Primary cutaneous amyloidosis
Primary systemic amyloidosis
Prolidase deficiency
Pseudoporphyria
Secondary cutaneous amyloidosis
Secondary systemic amyloidosis
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
more...
Autosomal recessive disorders
Lucey-Driscoll syndrome
Rotor syndrome
Glanzmann thrombasthenia
Dubin-Johnson syndrome
Lipidosis
Gangliosidosis
Genetic disorders
(15)
ALAD porphyria
Crigler-najjar syndrome
Nevoid basal cell carcinoma syndrome
Lucey-Driscoll syndrome
Rotor syndrome
Rotor syndrome
Porphyria
Hereditary coproporphyria
Variegate porphyria
Glanzmann thrombasthenia
Acute intermittent porphyria
Erythropoietic protoporphyria
Dubin-Johnson syndrome
Porphyria cutanea tarda
Lipidosis
Gangliosidosis
more...
Genetic disorder
ALAD porphyria
Rotor syndrome
Rare diseases
Glanzmann thrombasthenia
Acute intermittent porphyria
Lipidosis
Gangliosidosis
Diseases and disorders
(21)
Hereditary hyperbilirubinemia
Porphyrias
Porphyria congenital erythropoietic
Giant cell glioblastoma
Generalized flexion epilepsy
Generalized flexion epilepsy
Glycogenosis
Photosensitive epilepsy
Gastric cancer
Lucey-Driscoll syndrome
Hepatoeryt- hropoietic porphyria
Rotor syndrome
Porphyria
Neuraminidase deficiency
Hereditary coproporphyria
Variegate porphyria
Glanzmann thrombasthenia
Acute intermittent porphyria
Nevoid basal cell carcinoma syndrome
Porphyria cutanea tarda
Lipidosis
Gangliosidosis
more...
Tetrapyrroles
(38)
Heme
Hydroxymethylbilane
Porphyrin
Uroporphyrinogen III
Bilin (biochemistry)
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
Protoporphyrin IX
Talaporfin
Temoporfin
Tetraphenylporphine sulfonate
Tetrapheny- lporphyrin
Tetrapyrrole
Urobilin
Urobilinogen
Zinc protoporphyrin
more...
Tooth
(29)
Acid erosion
Cusp of Carabelli
Dens evaginatus
Dens invaginatus
Dental fluorosis
Dental fluorosis
Dentin dysplasia
Dentinogenesis imperfecta
Dilaceration
Enamel hypoplasia
External resorption
Hemolytic disease of the newborn
Hutchinson's teeth
Hypercementosis
Hyperdontia
Hypodontia
Internal resorption
Macrodontia (tooth)
Microdontia
Minocycline
Regional odontodysplasia
Supernumerary roots
Talon cusp
Taurodontism
Tea
Tetracycline
Tobacco
Tooth fusion
Tooth gemination
Turner's hypoplasia
more...
See also
(20)
Heme metabolism intermediates
Porphyria, hepatic
Anatomist
Body worlds
Dr Gunther von Hagens
Dr Gunther von Hagens
Porphyrin metabolism
Professor John Lee
Uroporphyrinogen III synthase
Gunther
Johnny Gunther
Plastination
Erythropoietic
Health Visitors
Human bodies
Trailblazing
Impregnation
Autosomal dominant
Autosomal recessive
Body donation
Bodily fluids
more...
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