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Choking and Blurred vision and Impaired vision and Pain and Redness and Skin symptoms
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Choking and Blurred vision and Impaired vision and Pain and Redness and Skin symptoms

  • Choking AND Blurred vision AND Impaired vision AND Pain AND Redness AND Skin symptoms - Causes of All Symptoms
  • Choking OR Blurred vision OR Impaired vision OR Pain OR Redness OR Skin symptoms - 9094 causes

Choking:

Blurred vision:

Impaired vision:

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Redness:

Skin symptoms:

Results: Causes of Choking AND Blurred vision AND Impaired vision AND Pain AND Redness AND Skin symptoms

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

Results: 9094 causes of Choking OR Blurred vision OR Impaired vision OR Pain OR Redness OR Skin symptoms

    1. 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 »
    2. 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 »
    3. 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 »
    4. 2-hydroxyethyl methacrylate sensitization
     A condition where exposure to 2-hydroxyethyl methacrylate results in sensitization to the chemical - further exposure to the chemical causes a reaction. The chemical is used in dental work so dental patients and dental workers are at risk of becoming sens...more »
    5. 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 »
    6. 2q deletion
     A rare chromosomal disorder where part of the long arm (q) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    7. 3 alpha methylglutaconicaciduria, type 3
     A rare genetic condition where a gene mutation prevents the production of certain protein which leads to a build-up of an acid (3-methylglutaconic acid) which can have a negative impact on the body. The condition is characterized mainly by damage to the o...more »
    8. 3-methylglutaconic aciduria, type 4
     A rare genetic disorder where the body's cells are unable to make sufficient energy resulting in an accumulation in the body of 3-methylglutaconic acid. Type 4 is characterized by symptoms which overlap type 1 and 3....more »
    9. 3?-hydroxysteroid dehydrogenase deficiency
     A ver rare form of congenital adrenal hyperplasia involving a deficiency of 3?-hydroxysteroid dehydrogenase which results in reduced production of adrenal steroids (mineralocorticoids, sex steroids and glucocorticoids). The disorder can occur in classical...more »
    10. 3C syndrome
     A rare disorder characterized by cardiac malformations, cerebellar hypoplasia and cranial dysmorphism which gives the disease it's name....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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