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Body symptoms and Brain symptoms and Combination of rigidity and tremor in both arms and Emotional lability and Hand paresthesia and Movement symptoms
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Body symptoms and Brain symptoms and Combination of rigidity and tremor in both arms and Emotional lability and Hand paresthesia and Movement symptoms

  • Body symptoms AND Brain symptoms AND Combination of rigidity and tremor in both arms AND Emotional lability AND Hand paresthesia AND Movement symptoms - Causes of All Symptoms
  • Body symptoms OR Brain symptoms OR Combination of rigidity and tremor in both arms OR Emotional lability OR Hand paresthesia OR Movement symptoms - 9212 causes

Body symptoms:

Brain symptoms:

Combination of rigidity and tremor in both arms:

Emotional lability:

Hand paresthesia:

Movement symptoms:

Results: Causes of Body symptoms AND Brain symptoms AND Combination of rigidity and tremor in both arms AND Emotional lability AND Hand paresthesia AND Movement symptoms

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

Results: 9212 causes of Body symptoms OR Brain symptoms OR Combination of rigidity and tremor in both arms OR Emotional lability OR Hand paresthesia OR Movement symptoms

    1. 10q Partial Trisomy
     A very rare genetic disorder characterized by the duplication of genetic material from the long arm (q) of chromosome 10 - the genetic material occurs three times in body cells instead of the normal two. The type and severity of symptoms may vary consider...more »
    2. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    3. 18p minus syndrome
     A rare chromosomal disorder where a portion of chromosome 18 is missing which is characterized by mental and growth deficiencies, drooping upper eyelid and prominent ears. The type and severity of symptoms is determined by the amount of genetic material t...more »
    4. 1q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    5. 1q terminal deletion
     A rare chromosomal disorder where the terminal part of the long arm (q) of chromosome 1 is deleted resulting in various abnormalities....more »
    6. 2-Hydroxyglutaricaciduria
     A rare metabolic disorder characterized by high levels of a certain chemical (2-Hydroxyglutaric) which causes a serious progressive neurological disease and damage to the brain. The features of this disorder are variable and some cases are milder than oth...more »
    7. 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-methylbu...more »
    8. 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-methylbu...more »
    9. 22q11.2 deletion syndrome
     A rare genetic disorder caused by the absence of a small portion of genetic material. A small section of chromosome 22 is missing at a location called q11.2. Chromosome 22 is one of 23 pairs of chromosomes that exist in humans....more »
    10. 2p21 deletion syndrome
     This syndrome is a more severe form hypotonia-cystinuria syndrome as a larger portion of genetic material from chromosome 2p21 is deleted. It is characterized by infant seizures, reduced muscle tone, developmental delay, lactic acidosis and unusual facial...more »

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  • Warning - Beta version - information may be incorrect (details)
  • Disclaimer - Do not use this information for diagnosis (details)
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