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Symptom Checker » Aphthous Ulcer » Mouth symptoms
 

Aphthous Ulcer and Mouth symptoms
Symptom Checker

Aphthous Ulcer and Mouth symptoms

Aphthous Ulcer:

Mouth symptoms:

Results: Causes of Aphthous Ulcer AND Mouth symptoms

    1. Agranulocytosis
     Total lack of granulocytes in the blood...read more »
    2. Behcet's Disease
     Recurring inflammation of small blood vessels affecting various areas....read more »
    3. Bejel
     An infectious disease caused by Treponema pallidum which is similar to the organism that causes syphilis but is not sexually transmitted....read more »
    4. Candidiasis
     Fungal infection of moist areas such as mouth or vagina...read more »
    5. Celiac Disease
     Digestive intolerance to gluten in the diet....read more »
    6. Chemical poisoning -- Sulfuric Acid
     Sulfuric Acid is a chemical used mainly in car batteries and in the fur and leather industries. It is a significant component of air pollution and results in the production of "acid rain". Ingestion and other exposures to the chemical can cause various sy...read more »
    7. Crohn's disease
     Crohn's disease causes inflammation of the digestive system. It is one of a group of diseases called inflammatory bowel disease. The disease can affect any area from the mouth to the anus. It often affects the lower part of the small intestine called the ...read more »
    8. Duodenal ulcer
     A peptic ulcer is erosion in the lining of the stomach or duodenum (the first part of the small intestine). The word "peptic" refers to pepsin, a stomach enzyme that breaks down proteins. If a peptic ulcer is located in the stomach it is called a gastric ...read more »
    9. Folate deficiency
    10. HIV/AIDS
     HIV is a sexually transmitted virus and AIDS is the progressive immune failure that HIV causes....read more »

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Results: 6667 causes of Aphthous Ulcer OR Mouth symptoms

    1. 14q+ syndrome
     A rare chromosomal disorder involving duplication of genetic material from the long arm (q) of chromosome 14 resulting in various abnormalities....more »
    2. 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 »
    3. 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 »
    4. 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 »
    5. 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 »
    6. 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 »
    7. 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 »
    8. 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 »
    9. 2q22-q24 deletion
     A rare chromosomal disorder where part of the long arm (q22-q24) of chromosome 2 is deleted resulting in various abnormalities which are determined by the size of the deleted portion....more »
    10. 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 »

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Notes About Causes

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