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Symptoms » Standing symptoms » Glossary
 

Glossary for Standing symptoms

Medical terms related to Standing symptoms or mentioned in this section include:

  • 2-Methylbutyric Aciduria: A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbutyryl-coenzyme A dehydrogenase) needed to convert the amino acid isoleucine into energy. 2-methylbutyrylglycine levels build up in the body and may cause damage. Symptoms vary according to the degree of enzyme deficiency - can range from asymptomatic to life-threatening.
  • 2-methylbutyryl-coenzyme A dehydrogenase deficiency: A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbutyryl-coenzyme A dehydrogenase) needed to convert the amino acid isoleucine into energy. 2-methylbutyrylglycine levels build up in the body and may cause damage. Symptoms vary according to the degree of enzyme deficiency - can range from asymptomatic to life-threatening.
  • Agenesis of the corpus callosum: Congenital absence of connective part of the brain.
  • Akathisia: A condition characterized by a constant urge to move resulting in the sufferer being unable to sit still. Can be caused by use of anti-psychotic drugs or anti-depressants or can occur spontaneously.
  • Alcohol abuse: Excessive alcohol as a symptom of other conditions
  • Anemia: Reduced red blood cells in the blood
  • Blood vessel symptoms: Symptoms affecting the blood vessels
  • Body symptoms: Symptoms affecting the entire body features.
  • Brain symptoms: Symptoms affecting the brain
  • Clubfoot: A deformity of the foot where there is a curled shape of the ankle, heels and toes.
  • Deep vein thrombosis: The formation of a thrombosis in the deep veins usually within the legs
  • Dermatomyositis: A muscle disease characterized by chronic muscle inflammation resulting in progressive muscle weakness and a characteristic rash.
  • Developmental delay due to 2-methylbutyryl-CoA dehydrogenase deficiency: A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbutyryl-coenzyme A dehydrogenase) needed to convert the amino acid isoleucine into energy. 2-methylbutyrylglycine levels build up in the body and may cause damage. Symptoms vary according to the degree of enzyme deficiency - can range from asymptomatic to life-threatening.
  • Duchenne Muscular Dystrophy: An inherited degenerative disease of the muscles which progresses rapidly compared to other muscle wasting diseases.
  • Head symptoms: Symptoms affecting the head or brain
  • Idiopathic myopathy: A rare condition involving inflammation of the skeletal muscles which become weak and wasted.
  • Movement symptoms: Changes to movement or motor abilities
  • Multiple pterygium syndrome: A very rare disorder characterized by webbing of various parts of the body, contractures, short stature, fusion of neck vertebrae and facial anomalies.
  • Muscle symptoms: Symptoms affecting the muscles of the body
  • Muscular Dystrophy: Any of various muscle wasting diseases
  • Musculoskeletal symptoms: Symptoms affecting muscles or bones of the skeleton.
  • Nerve symptoms: Symptoms affecting the nerves
  • Neurological symptoms: Any symptoms that are caused by neurological conditions
  • Olivopontocerebellar Atrophy: A group of diseases progressive degeneration occurs in a particular area of the brain (olivopontocerebellar area) which results in various neurological symptoms.
  • Orthostatic hypotension: also known as postural hypotension
  • Posture symptoms: Symptoms related to body posture
  • SBCAD deficiency: A very rare genetic disorder where an enzyme deficiency prevents the break down of certain proteins into energy and results in a harmful accumulation of acids in the blood and body tissues. More specifically, there is a deficiency of an enzyme (2-methylbutyryl-coenzyme A dehydrogenase) needed to convert the amino acid isoleucine into energy. 2-methylbutyrylglycine levels build up in the body and may cause damage. Symptoms vary according to the degree of enzyme deficiency - can range from asymptomatic to life-threatening.
  • Schwartz-Jampel Syndrome: A rare genetic disorder characterized by myotonia, blepharophimosis and joint limitation.
  • Spinal Muscular Atrophy type I: Type of SMA, a genetic motor neuron disease affecting nerves and muscles.
  • Spinal Muscular Atrophy type II: Type of SMA, a genetic motor neuron disease affecting nerves and muscles.
  • Spinal stenosis: Narrowing of the spinal cavity around the spinal cord.
  • Varicose veins: Appearance of veins in the skin
  • Walking symptoms: Problems with walking.

Conditions listing medical symptoms: Standing symptoms:

The following list of conditions have 'Standing symptoms' 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.

Select from the following alphabetical view of conditions which include a symptom of Standing symptoms or choose View All.

 

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