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Symptom Checker » Autonomic neuropathy » Fatigue with dyspnea
 

Autonomic neuropathy and Fatigue with dyspnea and Malabsorption
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Autonomic neuropathy and Fatigue with dyspnea and Malabsorption

  • Autonomic neuropathy AND Fatigue with dyspnea AND Malabsorption - Causes of All Symptoms
  • Autonomic neuropathy OR Fatigue with dyspnea OR Malabsorption - 225 causes

Autonomic neuropathy:

Fatigue with dyspnea:

Malabsorption:

Results: Causes of Autonomic neuropathy AND Fatigue with dyspnea AND Malabsorption

    1. Hereditary amyloidosis
     An inherited form of amyloidosis which is characterized by a build up of the protein amyloid in tissues and organs. This form of amyloidosis tends to affect mainly the nervous system and gastrointestinal tract. Symptoms are determined by the size and loca...read more »

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Note: Do not use for diagnosis; see limitations of results.

Results: 225 causes of Autonomic neuropathy OR Fatigue with dyspnea OR Malabsorption

    1. Abetalipoproteinemia
     A rare disorder involving abnormalities in fat metabolism. The resulting insufficiency of fats and vitamins affect the normal development and function of the body....more »
    2. Adult Panic-Anxiety Syndrome
     A psychiatric disorder involving anxiety and panic attacks that occur for no obvious reason....more »
    3. Amyloidosis beta2-microglobulinic
     Amyloidosis is a rare group of metabolic disorders where a protein called amyloid accumulates in body organs and tissues where it can cause damage. The type of amyloid protein involved in this type of amyloidosis is beta-2-microglobulin. The abnormal prot...more »
    4. Amyloidosis, Familial
     Amyloidosis is a rare group of metabolic disorders where a protein called amyloid accumulates in body organs and tissues where it can cause damage. In the familial form, the type of amyloid involved is usually a plasma protein called transthyretin. The ma...more »
    5. Amyloidosis, Inherited
     Amyloidosis is a rare group of metabolic disorders where a protein called amyloid accumulates in body organs and tissues where it can cause damage. In the inherited form, the type of amyloid involved is usually a plasma protein called transthyretin. The m...more »
    6. Anaphylaxis
     A rare, potentially life-threatening allergic reaction....more »
    7. Aplasia cutis congenital -- intestinal lymphangiectasia
     A rare disorder characterized by a skin defect and dilated intestinal lymph vessels....more »
    8. Arthrogryposis multiplex congenita -- pulmonary hypoplasia
     A rare congenital syndrome involving degeneration of the brain and spinal cord and characterized by facial, head, skeletal and muscular abnormalities. Reduced fetal activity causes many of the problems....more »
    9. Ascaris lumbricoides
     Common roundworm infecting human intestines. Causing restlessness, fever, diarrhea....more »
    10. Autoimmune enteropathy, type 1
     A rare condition involving autoimmune problems which can variably manifest as enteropathy (diarrhea), hemolytic anemia, and endocrine gland diseases such as diabetes mellitus and thyroid disease. Resistance to viral infections is poor. The condition is li...more »

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Notes About Causes

  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
  • Important - See your doctor - Only a doctor can give an accurate diagnosis (details)
 

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