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Rotor Syndrome
Rotor syndrome
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Topics Related to Rotor syndrome
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Hepatology
(15)
Dubin-Johnson syndrome
Crigler-najjar syndrome
Lucey-Driscoll syndrome
Bilirubin
Cholestasis
Cholestasis
Gilbert syndrome
Jaundice
Bile acid
Neonatal jaundice
Alpha 1 antitrypsin deficiency
Biliary
Urobilinogen
Primary sclerosing cholangitis
Cirrhosis
Gallstones
more...
Metabolic disorders
Leukodystrophy, globoid cell
Galactosemias
Crigler-najjar syndrome
Inborn errors of metabolism
Crigler-najjar syndrome
Leukodystrophy, globoid cell
Galactosemias
Genetic disorders
(18)
ALAD porphyria
Gunther disease
Hyperostosis, cortical, congenital
Adrenoleuk- odystrophy
Hereditary sensory and autonomic neuropathies
Hereditary sensory and autonomic neuropathies
Variegate porphyria
Hereditary coproporphyria
Acute intermittent porphyria
Erythropoietic protoporphyria
Porphyria cutanea tarda
Sickle cell anaemia
Dubin-Johnson syndrome
Crigler-najjar syndrome
Lucey-Driscoll syndrome
Leukodystrophy, globoid cell
Gilbert syndrome
Galactosemias
Alpha 1 antitrypsin deficiency
more...
Autosomal recessive disorders
Dubin-Johnson syndrome
Gunther disease
Lucey-Driscoll syndrome
Leukodystrophy, globoid cell
Sickle cell anaemia
Genetic disorder
ALAD porphyria
Gunther disease
Erythropoietic protoporphyria
Syndromes
Fetofetal transfusion
Carpal tunnel syndrome
Dubin-Johnson syndrome
Crigler-najjar syndrome
Lucey-Driscoll syndrome
Hereditary sensory and autonomic neuropathies
Gilbert syndrome
Medical condition
(50)
Hereditary hyperbilirubinemia
Glossopharyngeal nerve diseases
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Myopathies, structural, congenital
Enterocolitis, pseudomembranous
Physiologic nystagmus
Histiocytosis non-langerhans-cell
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Intervertebral disk displacement
Rosenthal syndrome
Brachial plexus neuropathies
Optic neuropathy, ischemic
Venous thromboembolism
Otosclerosis
Choledochal cyst
Hepatitis d
Kernicterus
Blood clots
Autoimmune hepatitis
Chloasma
Pulmonary embolism
Hepatitis e
Tendonitis
Tennis elbow
Carcinoma
Gunther disease
Hyperostosis, cortical, congenital
Cholestasis
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Fetofetal transfusion
Gilbert syndrome
Jaundice
Galactosemias
Variegate porphyria
Hereditary coproporphyria
Neonatal jaundice
Acute intermittent porphyria
Alpha 1 antitrypsin deficiency
Porphyria cutanea tarda
Sickle cell anaemia
Primary sclerosing cholangitis
Cirrhosis
Carpal tunnel syndrome
Gallstones
more...
Porphyrias
(10)
Erythropoietic porphyrias
Hepatoeryt- hropoietic porphyria
Porphyria, hepatic
ALAD porphyria
Acute intermittent porphyria
Acute intermittent porphyria
Erythropoietic protoporphyria
Hereditary coproporphyria
Porphyria
Porphyria cutanea tarda
Variegate porphyria
more...
Skin conditions resulting from errors in metabolism
(86)
Hypercarotenemia
Acute intermittent porphyria
Adrenoleuk- odystrophy
Alkaptonuria
Amyloid purpura
Amyloid purpura
Amyloidosis
Apolipoprotein B deficiency
B-mannosidase deficiency
CADASIL syndrome
Calcinosis cutis
Cerebrotendineous xanthomatosis
Citrullinemia
Combined hyperlipidemia
Diabetic bulla
Diabetic cheiroarthropathy
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
Gunther disease
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
Pseudoporphyria
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...
Metabolism
Heme metabolism intermediates
Coproporphyrin
Excretion
Bilirubin
Tetrapyrroles
(35)
Heme
Bilin (biochemistry)
Bilirubin
Bilirubin (data page)
Biliverdin
Biliverdin
Chlorophyll
Chlorophyll a
Chlorophyll b
Chlorophyll d
Chlorophyllin
Coproporphyrin
Coproporphyrinogen III
Corrole
Heme a
Heme b
Heme c
Heme o
Hydroxymethylbilane
Phycobilin
Phycocyanobilin
Phycoerythrobilin
Phycoerythrocyanin
Phycourobilin
Porphin
Protoporphyrin
Protoporphyrin IX
Talaporfin
Temoporfin
Tetraphenylporphine sulfonate
Tetrapheny- lporphyrin
Tetrapyrrole
Urobilin
Urobilinogen
Uroporphyrinogen III
Zinc protoporphyrin
more...
Medicine
Diseases and disorders
Heme arginate
Idiopathic
Porphyria, hepatic
Choledochal cyst
See also
(20)
Physiologic
Birth control
Porphyrin metabolism
Hemolysis
Sexual deviations
Sexual deviations
Levonorgestrel
Glucuronyl transferase
Autosomal
Gyroscope
Nsd Powerball
Power Ball
Liver biopsy
Conjugate vaccine
Rotor (mathematics)
Tumours
Estrone
Ethinylestradiol
UGT1A1
Cyproterone acetate
Cadmium
more...
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