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Symptoms » Easily fatigued » Glossary
 

Glossary for Easily fatigued

Medical terms related to Easily fatigued or mentioned in this section include:

  • Acid-Base Imbalance: A disruption to the normal acid-base equilibrium in the body. There are four main groups of disorder involving an acid-base imbalance: respiratory acidosis or alkalosis and metabolic acidosis or alkalosis. Obviously the severity of symptoms is determined by the degree of imbalance.
  • Acute tubulointerstitial nephritis and uveitis syndrome: The association of a sudden kidney disorder with eye inflammation. Autoimmune processes are believed to be involved.
  • Alcohol abuse: Excessive alcohol as a symptom of other conditions
  • Amyloidosis: A disease characterized by the accumulation of insoluble amyloid protein in tissues and organs which in turn affects the functioning of these tissues and organs.
  • Anxiety: Excessive worry, anxiety, or fear.
  • Aortic dilatation- joint hypermobility- arterial tortuosity: A rare syndrome characterized by the dilation of the aortic root, hyperextensible joints and varicose veins
  • Aortic supravalvular stenosis: A rare congenital condition involving increased intestinal calcium absorption and characterized by development delay, distinctive facial features, small nails and short stature.
  • Atrial Septal Defect 3: A rare heart malformation involving the presence of an abnormal opening between the two atrial chambers of the heart which allows abnormal mixing of oxygenated and deoxygenated blood. The severity of the symptoms depends on the size and location of the defect with mild cases being asymptomatic until adulthood. Atrial septal defect 3 is caused by a mutation on chromosome 14q12. There are no other heart abnormalities associated with the condition.
  • Atrial Septal Defect 4: A rare heart malformation involving the presence of an abnormal opening between the two atrial chambers of the heart which allows abnormal mixing of oxygenated and deoxygenated blood. The severity of the symptoms depends on the size and location of the defect with mild cases being asymptomatic until adulthood. Atrial septal defect 4 is caused by a mutation on chromosome 7p15-p14. There are no other heart abnormalities associated with the condition.
  • Atrial Septal Defect 5: A rare heart malformation involving the presence of an abnormal opening between the two atrial chambers of the heart which allows abnormal mixing of oxygenated and deoxygenated blood. The severity of the symptoms depends on the size and location of the defect with mild cases being asymptomatic until adulthood. Atrial septal defect 5 is caused by a mutation on chromosome 15q14. There are no other heart abnormalities associated with the condition.
  • Atrial Septal Defect 6: A rare heart malformation involving the presence of an abnormal opening between the two atrial chambers of the heart which allows abnormal mixing of oxygenated and deoxygenated blood. The severity of the symptoms depends on the size and location of the defect with mild cases being asymptomatic until adulthood. Atrial septal defect 6 is caused by a mutation on chromosome 4q32-q33.
  • Atrial septal defect 1: A rare heart malformation involving the presence of an abnormal opening between the two atrial chambers of the heart which allows abnormal mixing of oxygenated and deoxygenated blood. The severity of the symptoms depends on the size and location of the defect with mild cases being asymptomatic until adulthood. Atrial septal defect 1 is caused by a mutation on chromosome 6p21.3.
  • Atrial septal defect 2: A rare heart malformation involving the presence of an abnormal opening between the two atrial chambers of the heart which allows abnormal mixing of oxygenated and deoxygenated blood. The severity of the symptoms depends on the size and location of the defect with mild cases being asymptomatic until adulthood. Atrial septal defect 2 is caused by a mutation on chromosome 8p23.1-p22.
  • Body symptoms: Symptoms affecting the entire body features.
  • Brain symptoms: Symptoms affecting the brain
  • COPD: Severe obstruction of bronchial air flow typically from bronchitis and/or emphysema.
  • Calcification of basal ganglia with or without hypocalcemia: Calcification of a part of the brain called the basal ganglia. That calcification may be associated with conditions such as hypothyroidism, cytomegalovirus, and AIDS or may occur for no apparent reason. The severity of the condition may vary greatly from asymptomatic to neurological, psychiatric and movement disorders. The disorder may also progress at variable rates or remain stable depending on the underlying disease process.
  • Cataract and cardiomyopathy: A rare syndrome characterized by the association of congenital cataracts, heart muscle disease, lactic acidosis and skeletal muscle disease. The disorder involves the abnormal storage of lipids and glycogen in the skeletal and heart muscles. The cataracts progress rapidly and require surgery. The severity of the disorder ranges from stillbirth to survival into the fourth decade.
  • Chronic fatigue syndrome: A persistent debilitating fatigue of recent onset
  • Chronic pyelonephritis: chronic pyelonephritis is persistent kidney inflammation that can scar the kidneys and may lead to chronic renal failure
  • Common symptoms: The most common symptoms
  • Congestive cardiac failure: A condition characterized by breathlessness and abnormal sodium and water retention.
  • Depressive symptoms: Inappropriate depressed mood.
  • Eisenmenger Syndrome: Increased lung blood pressure that can result from conditions such as a hole in the wall between the two heart chambers.
  • Energy symptoms: Symptoms related to levels of energy.
  • Epiphyseal dysplasia, multiple: Abnormalities in the ends of a number of bones resulting in the early onset of osteoarthrosis and joint pain. There are 6 different subtypes of the disease, with each caused by a mutation in a different gene.
  • Epiphyseal dysplasia, multiple, 5: Abnormalities in the ends of a number of bones resulting in the early onset of osteoarthrosis and joint pain. The hips and knees were the main joints involved. It is caused by defects in the gene for matrilin-3 (MATN3).
  • Fatigue: Excessive tiredness or weakness.
  • Friedreich ataxia -- congenital glaucoma: A rare disorder characterized by glaucoma at birth and a progressive neuromuscular disorder.
  • Glycogen storage disease type 7: An inherited metabolic disorder where there is a deficiency of phosphofructokinase-1 in the muscle and a partial deficiency in red blood cells which prevents glucose being converted to energy during exercise.
  • Head symptoms: Symptoms affecting the head or brain
  • Hepatic failure: loss of normal liver function and metabolism of products by the liver
  • Hypercalcemia: Raised blood calcium levels
  • Hypertension in children: Hypertension in children is a condition in which a child has an abnormal elevation in blood pressure.
  • Hypertension in children from 11 through adolescence: Hypertension in children from 11 through adolescence refers to a child between the ages of 11 years through adolescence who has an abnormal elevation in blood pressure.
  • Hypertension in children one to ten years: Hypertension in children one to ten years refers to a child between the ages of one to ten years who has an abnormal elevation in blood pressure.
  • Hypocalcaemia: Decreased concentration of calcium in the blood.
  • Hypothyroidism: The decreased activity of the thyroid gland
  • Insomnia: feeling of melancholy
  • Ischemic heart disease: Heart disease from reduced blood flow to the heart
  • Leukemia: Cancer of the blood cells, usually white blood cells.
  • Low haemoglobin: Decreased concentration of haemoglobin in the blood.
  • Lymphoma: Any neoplastic disorder that occurs in lymphoid tissue
  • Movement symptoms: Changes to movement or motor abilities
  • Muscle symptoms: Symptoms affecting the muscles of the body
  • Muscle weakness: Weakness of the muscles or loss of tone
  • Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
  • Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency: A genetic, nonprogressive neuromuscular disorder causing muscle weakness. The severity of symptoms is variable and stress and illness can exacerbate symptoms.
  • Myasthenic syndrome, congenital, slow-channel: A rare disorder involving progressive muscle wasting and weakness of variable severity depending on the exact origin of the genetic defect. The problem arises from defective processes at the junction of nerve and muscle cells.
  • Myopathy, Myofibrillar, BAG3-Related: An early-onset, progressive muscle disease.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurological symptoms: Any symptoms that are caused by neurological conditions
  • Neuropathy, hereditary motor and sensory, LOM type: A severe form of Charcot-Marie-Tooth disease which involves the loss of the protective covering around nerves resulting in various nerve problems. Muscle weakness and wasting and sensory loss is more severe in the ends of the arms and legs.
  • Obesity: Excessive body weight especially fat.
  • Pain: Any type of pain sensation symptoms.
  • Polymyalgia rheumatica: A condition characterized by muscle pain and stiffness, fatigue and fever. It is often associated with giant-cell arteritis which is a related but more serious condition.
  • Pseudohypoparathyroidism: An inherited disorder where the body is unable to respond to the parathyroid hormone even though there are normal levels of it. Impaired bone growth is the main feature of this disorder.
  • Renal failure: A condition characterized by a failure of the kidney to excrete toxic metabolites from the body
  • Respiratory acidosis: respiratory acidosis is acidosis (abnormally increased acidity of the blood) due to decreased ventilation of the pulmonary alveoli, leading to elevated arterial carbon dioxide concentration
  • Sarcoidosis: Rare autoimmune disease usually affecting the lungs.
  • Sensations: Changes to sensations or the senses
  • Sensory symptoms: Symptoms affecting the sensory systems.
  • Sick: Feeling ill or off color
  • Spontaneous pneumothorax, familial type: A rare inherited disorder which causes the lungs to collapse spontaneously.
  • Systemic lupus erythematosus: chronic autoimmune disease that can be fatal, though with recent medical advances, fatalities are becoming increasingly rare.
  • Timme syndrome: A syndrome involving insufficiency of the thymus, adrenal and pituitary glands. The disorder has involves three phases, each of which has varying symptoms: phase 1 is before puberty, phase 2 occurs after puberty and phase 3 tends to occur in the third decade.
  • Type VII Glycogen Storage Disease: A condition which is characterized by a disease affecting glycogen storage
  • Weakness: Symptoms causing weakness of the body

Conditions listing medical symptoms: Easily fatigued:

The following list of conditions have 'Easily fatigued' or similar listed as a symptom in our database. This computer-generated list may be inaccurate or incomplete. Always seek prompt professional medical advice about the cause of any symptom.

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Conditions listing medical complications: Easily fatigued:

The following list of medical conditions have 'Easily fatigued' or similar listed as a medical complication in our database.

 

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