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Abrupt loss of vision in one eye and Eye symptoms and Neovascular glaucoma in both eyes and Neovascular glaucoma in one eye and Nerve symptoms
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Results: Causes of Abrupt loss of vision in one eye AND Eye symptoms AND Neovascular glaucoma in both eyes AND Neovascular glaucoma in one eye AND Nerve symptoms

    1. Eales Disease
     A rare eye disorder characterized by sudden vision loss, problems with eye blood vessuls and reoccurring eye blood vessel hemorrhages as well as oozing of clear thick fluid from inside the eyeball. Usually occurs after a stressful situation, trauma or aft...read more »

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Results: 10934 causes of Abrupt loss of vision in one eye OR Eye symptoms OR Neovascular glaucoma in both eyes OR Neovascular glaucoma in one eye OR Nerve symptoms

    11. 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 »
    12. 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 »
    13. 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 »
    14. 3-Hydroxyacyl-CoA Dehydrogenase II Deficiency
     A rare genetic disorder involving the deficiency of an enzyme (hydroxyacyl-coa dehydrogenase). The severity of the symptoms is highly variable with some cases resulting in death during the first decade while others suffer psychomotor and regression. Sympt...more »
    15. 3-Hydroxyisobutyric aciduria
     A rare inborn metabolic disorder which causes brain and facial anomalies, seizures and growth problems....more »
    16. 3-M Syndrome
     A rare genetic condition which is characterized by distinctive physical features and severe growth retardation that starts during the fetal stage. Intelligence is not affected....more »
    17. 3-alpha-Hydroxyacyl-CoA Dehydrogenase Deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    18. 3-alpha-hydroxyacyl-coenzyme A dehydrogenase deficiency
     A rare inherited form of biochemical disorder characterized by the deficiency of a particular enzyme (3-Hydroxyacyl-CoA Dehydrogenase). The enzyme deficiency only affects certain body tissues, in particular the skeletal muscles. The lack of enzyme activit...more »
    19. 3-alpha-hydroxyisobutyryl-CoA hydrolase deficiency
     A metabolic disorder involving an enzyme deficiency which causes symptoms such as degeneration of the nervous system. The other features of the disorder are somewhat variable....more »
    20. 3-methylglutaconic aciduria, type 1
     A recessively inherited metabolic disorder characterized by methylglutaconic acid in the urine....more »

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  • Warning - Beta version - information may be incorrect (details)
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