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Differential Diagnosis For Glucose, blood (Lab) - Decreased: Metabolic, Storage Disorders
List of current finding(s):
Glucose, blood (Lab) - Decreased
- Electromagnetic, Physics, trauma, Radiation Causes (1)
- Surgical, Procedure Complication (1)
- Infectious Disorders (Specific Agent) (7)
- Infected organ, Abscesses (2)
- Neoplastic Disorders (22)
- Allergic, Collagen, Auto-Immune Disorders (7)
- Metabolic, Storage Disorders (23)
- Biochemical Disorders (3)
- Deficiency Disorders (5)
- Hereditary, Familial, Genetic Disorders (2)
- Usage, Degenerative, Necrosis, Age Related Disorders (1)
- Relational, Mental, Psychiatric Disorders (6)
- Anatomic, Foreign Body, Structural Disorders (1)
- Arteriosclerotic, Vascular, Venous Disorders (4)
- Functional, Physiologic Variant Disorders (5)
- Vegetative, Autonomic, Endocrine Disorders (17)
- Reference to Organ System (15)
- Idiopathic, Unclassified Disorders (1)
- Pathophysiologic (1)
- Heirarchical Major Groups (1)
- Drugs (26)
- Poisoning (Specific Agent) (9)
- Organ Poisoning (Intoxication) (1)
- Synonyms (6)
- Definition
- External Links Related to Glucose, blood (Lab) - Decreased
- Metabolic, Storage Disorders:
- Hypoglycemia, reactive diabetic
- Enzyme defect/deficiency disorders
- Infant of diabetic mother
- Nocturnal hypoglycemia/insulin
- Metabolic disorders
- Pyruvate carboxylase enzyme deficiency/PCD
- LCHAD/Long chain OH-CoA dehydrogenase def
- Leucine-sensitive hypoglycemia syndrome
- MCAD/Medium chain OH-CoA Dehydrogenase def
- VLCHAD/Very Long chain OH-CoA dehydrogenase def
- Amylopectinosis (Andersen's) disease (GSD IV)
- Carnitine deficiency syndrome
- Forbes disease (Cori disease, III)
- Fructose 1,6 diphosphatase deficiency
- Fructose intolerance, hereditary
- Galactosemia
- Glycogen storage diseases
- Glycogen synthetase deficiency
- Liver Phosphorylase deficiency
- Maple syrup urine disease
- McArdle's syndrome
- Phosphoenolpyruvate carboxykinase defic (PEPCK)
- Von Gierke's disease/glycogenosis I
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