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Symptom Checker » Presence of Heinz bodies in blood smear » Women's health symptoms
 

Presence of Heinz bodies in blood smear and Women's health symptoms
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Presence of Heinz bodies in blood smear and Women's health symptoms

  • Presence of Heinz bodies in blood smear AND Women's health symptoms - Causes of All Symptoms
  • Presence of Heinz bodies in blood smear OR Women's health symptoms - 1151 causes

Presence of Heinz bodies in blood smear:

Women's health symptoms:

Results: Causes of Presence of Heinz bodies in blood smear AND Women's health symptoms

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Results: 1151 causes of Presence of Heinz bodies in blood smear OR Women's health 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. 3-Beta-HSD, Deficiency of
     A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wast...more »
    3. 3-Beta-Hydroxysteroid Dehydrogenase deficiency
     A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wast...more »
    4. 3-Beta-Hydroxysteroid Dehydrogenase, Type II, Deficiency of
     A rare condition where the deficiency of a particular enzyme (3-Beta-Hydroxysteroid Dehydrogenase) results in reduced levels of adrenal hormones - mineralocorticoids, glucocorticoids and sex steroids. The condition results in variable degrees of salt wast...more »
    5. 3-Hydroxyisobutyric aciduria
     A rare inborn metabolic disorder which causes brain and facial anomalies, seizures and growth problems....more »
    6. 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 »
    7. 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 »
    8. 46,XX Gonadal dysgenesis epibulbar dermoid
     A rare disorder characterized by gonad abnormalities and an eye disorder called epibulbar dermoid....more »
    9. 46,XX chromosome 7 deletion p13-p21
     A chromosomal disorder where a small portion of chromosome 7 is deleted which results in a range of abnormalities....more »
    10. 46,XX testicular disorder of sex development
     A sex chromosome disorder in males which affects gonadal development and causes infertility. Males have XX chromosomes instead of the normal XY....more »

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