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Glucose 6 Phosphate Dehydrogenase Deficiency
Glucose 6 phosphate dehydrogenase deficiency
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Hematology
Hemolytic anemia
Hemolysis
Pyruvate kinase deficiency
Neonatal hyperbilirubinemia
Hematologic disease
Acquired hemolytic anemia
Activated protein c resistance
Diseases and disorders
(30)
Gonadotropin deficiency
Gyrate atrophy
Mesangial proliferative glomerulonephritis
Ileocolitis
Globoid cell leukodystrophy
Globoid cell leukodystrophy
Gluten enteropathy
Glossopharyngeal neuralgia
Post-streptococcal glomerulonephritis
Gonococcal
Glomerulonephritis, membranopr- oliferative
Goodpastures Syndrome
Granulomatous
Thrombasthenia
Bacteremia
Methemoglobinemia
Kernicterus
Glycogen storage disease type iib
Alport syndrome
Sideroblastic
GSD type IV
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glycogen storage disease
Hyperbilirubinemia
Malaria
Anemias
Hemolytic anemia
Pyruvate kinase deficiency
Neonatal hyperbilirubinemia
Hematologic disease
Activated protein c resistance
more...
Inborn errors of metabolism
(9)
Glycogen storage disease type v
GSD type I
3 methylcrotonyl-coa carboxylase deficiency
GSD type III
Globoid cell leukodystrophy
Globoid cell leukodystrophy
Pyruvate kinase deficiency
Glycogen storage disease type iib
Galactose-- 1-phosphate uridylyltransferase galactosemia
Glycogen storage disease
more...
Autosomal recessive disorders
(9)
Glycogen storage disease type v
Globoid cell leukodystrophy
Thrombasthenia
GSD type I
Methemoglobinemia
Methemoglobinemia
3 methylcrotonyl-coa carboxylase deficiency
Glycogen storage disease type iib
GSD type III
Galactose-- 1-phosphate uridylyltransferase galactosemia
more...
Genetic disorders
(17)
Aicardi syndrome
Adrenoleuk- odystrophy
Glycogen storage disease type v
Ileocolitis
Globoid cell leukodystrophy
Globoid cell leukodystrophy
Thrombasthenia
GSD type I
Pyruvate kinase deficiency
Methemoglobinemia
3 methylcrotonyl-coa carboxylase deficiency
Glycogen storage disease type iib
Alport syndrome
Sideroblastic
GSD type IV
GSD type III
Activated protein c resistance
Galactose-- 1-phosphate uridylyltransferase galactosemia
more...
Inflammations
Glossitis
Glomerulonephritis, membranous
Vaginal atrophy
Ileocolitis
Glomerulonephritis, membranopr- oliferative
World Health Organization essential medicines
(8)
Cotrimoxazole
Chloroquine phosphate
Trimethoprim
Nitrofurantoin
Dapsone
Dapsone
Marcaine
Sulfadiazine
Quinine
more...
Sulfonamide antibiotics
(26)
Flamazine
Mafenide
Sulfa
Sulfacetamide
Sulfamethoxazole
Sulfamethoxazole
Sulfisoxazole
Aldesulfone sodium
Elixir sulfanilamide incident
Prontosil
Sulfadimethoxine
Sulfadimidine
Sulfalene
Sulfamazone
Sulfamerazine
Sulfamethizole
Sulfametho- xypyridazine
Sulfametomidine
Sulfametoxydiazine
Sulfametrole
Sulfamoxole
Sulfaperin
Sulfaphenazole
Sulfapyridine
Sulfathiourea
Sulfatolamide
Sulfisomidine
more...
Antimalarial agents
(36)
Hydroxychloroquine
Primaquine
Pyrimethamine
Sulfadoxine
8-Aminoquinoline
8-Aminoquinoline
ASAQ
Amodiaquine
Antimalarial drug
Artelinic acid
Artemether
Artemisinin
Artemotil
Artenimol
Artesunate
Artesunate suppositories
Atovaquone
Azithromycin
Chloroquine phosphate
Chlorproguanil
Chlorproguanil hydrochlor- ide-dapsone-artesunate
Coartem
Cotrifazid
Cycloguanil
Dihydroartemisinin
Doxycycline
Halofantrine
Lapdap
Lumefantrine
Mefloquine
Pamaquine
Piperaquine
Proguanil
Pyronaridine
Quinacrine
Quinine
Tafenoquine
more...
Inborn error of metabolism
(75)
Granulomatous thyroiditis
Hunter syndrome
Inborn errors of amino acid metabolism
Inborn errors of purine-pyrimidine metabolism
Lesch–Nyhan syndrome
Lesch–Nyhan syndrome
Menkes disease
Oculocerebrorenal syndrome
Ornithine transcarbamylase deficiency
Pyruvate dehydrogenase deficiency
2-Hydroxyglutaric aciduria
Abscess of thymus
Acute infectious thyroiditis
Adiposogenital dystrophy
Adrenalitis
Adrenocortical hyperfunction
Adrenocorticotropic hormone deficiency
Albright's hereditary osteodystrophy
Aldolase A deficiency
Amyloid degeneration
Autoimmune adrenalitis
Autoimmune thyroiditis
Biotin deficiency
Diabetes complication
Diabetes mellitus and deafness
Diabetic amyotrophy
Endocrine bone disease
Endocrine paraneoplastic syndrome
Enolase deficiency
Essential fructosuria
Fatty-acid metabolism disorder
Finnish type amyloidosis
GSD type 0
GSD type IV
Glucocorticoid deficiency 1
Glycogen storage disease type VI
Glycogen storage disease type XI
Glycoproteinosis
Histidinemia
Hyperinsulinemia
Hyperpituitarism
Hypoestrogenism
Hypophysitis
Hypothalamic disease
Idiopathic hypoglycemia
Impaired fasting glycaemia
Juvenile diabetes mellitus
Keshan disease
MODY 1
MODY 2
MODY 3
MODY 4
MODY 5
MODY 6
Methylmalonyl-CoA mutase deficiency
Ochronosis
Parathyroiditis
Pentosuria
Permanent neonatal diabetes mellitus
Piebaldism
Pituitary ACTH hypersecretion
Pituitary disease
Postpartum thyroiditis
Pseudohypo- aldosteronism
Pseudohypo- parathyroidism
Sheehan's syndrome
Sphincter of Oddi dysfunction
Subacute thyroiditis
Tertiary hyperparathyroidism
Testicular disease
Thymic hypoplasia
Thyroid dyshormonogenesis
Toxic multinodular goitre
Toxic nodular goitre
Transaldolase deficiency
Vitamin poisoning
more...
Drug
(17)
Urogesic
Bactrim DS
Pyridium Plus
Fansidar
Glyoxide
Glyoxide
Phenazo
Bactrim Pediatric
Septra DS
Baridium
Cotrim DS
Pyridiate
Quinine Sulfate
Sulfatrim
Urodine
Azo-Standard
Sulfametho- xazole-Trimethoprim
Sulfadiazine
more...
Symptoms
(11)
Decreased appetite
Bluish fingernails
Joint aches
Dark urine
Hemoglobinuria
Hemoglobinuria
Pallor
Shortness of breath
Splenomegaly
Tachycardia
Yellow skin color
Diaherria
more...
Causes, incidence, and risk factors
Acute
Chronic
Spherocytosis
Hemolytic anemia
Anemia
Signs and tests
(9)
Reticulocyte
Bilirubin
Hemoglobin
LDH
Methemoglobin reduction
Methemoglobin reduction
Methylene blue test
Peripheral
Red blood cell count
Serum haptoglobin
more...
See also
(20)
Glucose-6-phosphate dehydrogenase
Glucuronyl transferase
Glucocerebroside
Glucose 6-phosphate
Pentose phosphate pathway
Pentose phosphate pathway
Pyrethrum
Phenazopyridine
Galactose metabolism
Magnesium trisilicate
Glucose 6-phosphatase
Medicine
Quinolone antibiotics
Lomefloxacin
Methemoglobin
Milk fruit
Hyper IgM Syndrome Type 1
Kaolin
Gierke
Chemical substances
Sulfonamides
more...
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