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Pages in category "Inborn errors of metabolism"
The following 200 pages are in this category, out of 277 total.
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A
- Acid lipase disease
- Acidosis
- Acrodermatitis enteropathica
- Adenylosuccinate lyase deficiency
- Aldolase A deficiency
- Alkalosis
- Alkaptonuria
- Alkaptonuria (patient information)
- Alpha 1-antitrypsin deficiency (patient information)
- Alpha-ketoglutarate dehydrogenase deficiency
- Alpha-mannosidosis
- List of amino acid metabolism disorders
- Amyloidosis (patient information)
- Analbuminaemia
- Anion gap
- Arakawa's syndrome II
- Arginemia
- Aspartylglucosaminuria
C
D
- Danon disease
- Dehydration
- Dehydration (patient information)
- Dehydration case study one
- Dehydration causes
- Dehydration classification
- Dehydration cost-effectiveness of therapy
- Dehydration differential diagnosis
- Dehydration electrocardiogram
- Dehydration epidemiology and demographics
- Dehydration future or investigational therapies
- Dehydration historical perspective
- Dehydration history and symptoms
- Dehydration laboratory findings
- Dehydration medical therapy
- Dehydration MRI
- Dehydration natural history, complications and prognosis
- Dehydration other diagnostic studies
- Dehydration other imaging findings
- Dehydration overview
- Dehydration pathophysiology
- Dehydration physical examination
- Dehydration primary prevention
- Dehydration risk factors
- Desmosterolosis
- Dihydropyrimidine dehydrogenase deficiency
- Disaccharidase
- Disorders of calcium metabolism
E
F
- Fabry's disease
- Fabry's disease MRI
- Familial hypercholesterolemia
- Familial mediterranean fever
- Familial mediterranean fever (patient information)
- Familial mediterranean fever case study one
- Familial mediterranean fever causes
- Familial mediterranean fever cost-effectiveness of therapy
- Familial mediterranean fever epidemiology and demographics
- Familial mediterranean fever future or investigational therapies
- Familial mediterranean fever historical perspective
- Familial mediterranean fever history and symptoms
- Familial mediterranean fever laboratory findings
- Familial mediterranean fever laboratory Findings
- Familial mediterranean fever medical therapy
- Familial mediterranean fever natural history, complications and prognosis
- Familial mediterranean fever other diagnostic studies
- Familial mediterranean fever overview
- Familial mediterranean fever pathophysiology
- Familial mediterranean fever physical examination
- Familial mediterranean fever prevention
- Familial mediterranean fever risk factors
- Fanconi syndrome
- Farber disease
- Inborn errors of lipid metabolism
- List of fatty acid metabolism disorders
- Fructose bisphosphatase deficiency
- Fumarase deficiency
G
- Galactokinase deficiency
- Galactose-1-phosphate uridylyltransferase galactosemia
- Galactosemia differential diagnosis
- Gangliosidosis
- Glucose-galactose malabsorption
- Glutaric acidemia type 2
- Glycogen storage disease type I (patient information)
- Glycogen storage disease type I case study one
- Glycogen storage disease type II (patient information)
- Glycogen storage disease type II case study one
- Glycogen storage disease type III (patient information)
- Glycogen storage disease type XI
- GM1 gangliosidoses
- GM2 gangliosidoses
- Guanidinoacetate methyltransferase deficiency
H
- Hawkinsinuria
- Hepatoerythropoietic porphyria
- Holocarboxylase synthetase deficiency
- Hunter syndrome (patient information)
- Hunter syndrome case study one
- Hurler syndrome (patient information)
- Hurler syndrome case study one
- Hurler syndrome classification
- Hyperammonemia
- Hyperchloremia
- Hyperchloremia (patient information)
- Hyperchloremia case study one
- Hyperchloremia causes
- Hyperchloremia classification
- Hyperchloremia differential diagnosis
- Hyperchloremia epidemiology and demographics
- Hyperchloremia history and symptoms
- Hyperchloremia laboratory findings
- Hyperchloremia medical therapy
- Hyperchloremia natural history, complications and prognosis
- Hyperchloremia other diagnostic studies
- Hyperchloremia overview
- Hyperchloremia pathophysiology
- Hyperchloremia physical examination
- Hyperchloremia primary prevention
- Hyperchloremia risk factors
- Hyperlysinemia
- Hypermagnesemia
- Hypermagnesemia (patient information)
- Hypermagnesemia case study one
- Hypermagnesemia causes
- Hypermagnesemia differential diagnosis
- Hypermagnesemia electrocardiogram
- Hypermagnesemia epidemiology and demographics
- Hypermagnesemia historical perspective
- Hypermagnesemia history and symptoms
- Hypermagnesemia laboratory findings
- Hypermagnesemia medical therapy
- Hypermagnesemia natural history, complications and prognosis
- Hypermagnesemia overview
- Hypermagnesemia pathophysiology
- Hypermagnesemia physical examination
- Hypermagnesemia ultrasound
- Hypermethioninemia
- Hypernatremia
- Hypernatremia (patient information)
- Hypernatremia case study one
- Hypernatremia causes
- Hypernatremia CT
- Hypernatremia dietary management
- Hypernatremia electrocardiogram
- Hypernatremia epidemiology and demographics
- Hypernatremia history and symptoms
- Hypernatremia laboratory findings
- Hypernatremia laboratory tests
- Hypernatremia medical therapy
- Hypernatremia MRI
- Hypernatremia natural history
- Hypernatremia natural history, complications and prognosis
- Hypernatremia other diagnostic studies
- Hypernatremia overview
- Hypernatremia pathophysiology
- Hypernatremia physical examination
- Hypernatremia primary prevention
- Hypernatremia risk factors
- Hypernatremia secondary prevention
- Hypernatremia surgery
- Hyperprolinemia
- Hyperuricemia
- Hypervalinemia
- Hypervolemia
- Hypochloremia
- Hypokalemia electrocardiogram
- Hypokalemia history and symptoms