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Symptom Checker » Thyroid problems » Umbilical hernia
 

Thyroid problems and Umbilical hernia
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Thyroid problems and Umbilical hernia

Thyroid problems:

Umbilical hernia:

Results: Causes of Thyroid problems AND Umbilical hernia

Results: 254 causes of Thyroid problems OR Umbilical hernia

    1. 17-Beta-hydroxysteroid dehydrogenase III deficiency
     A rare disorder characterized caused by an enzyme (17-ketosteroid reductase) defect only in the testes which results in a lack of testosterone which is needed during the fetal stage to give males there physical characteristics....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. 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 »
    4. Achard-Thiers Syndrome
     A hormonal disorder that occurs in diabetic postmenopausal women. It is characterized by diabetes mellitus and hirsuitism....more »
    5. Achondrogenesis type 1A and 1B
     A rare lethal genetic disorder characterized by a low nasal bridge, very short limbs and incomplete bone formation of lower spine....more »
    6. Achondroplasia regional -- dysplasia abdominal muscle
     A rare syndrome characterized mainly by abnormal bone development of the ilium, ribs and abdominal muscles. The abdominal muscles tend to become more develope with increasing age....more »
    7. Acrocallosal Syndrome (Schinzel Type)
     A rare condition characterized by absence of portion of the brain (corpus callosum), mental deficiency, duplicated toes, mental deficiency and other abnormalities....more »
    8. Acrocephalopolydactyly II
     A rare genetic disorder characterized by head, hand and genital anomalies as well as mental retardation....more »
    9. Acrocephalopolysyndactyly, type 2 (ACPS 2)
     A rare genetic disorder characterized by premature closing of skull bones, craniofacial abnormalities, heart defects, growth retardation and other disorders....more »
    10. Acroosteolysis dominant type
     A rare inherited connective tissue disorder characterized by breakdown of bone especially in the ends of the fingers and toes....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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