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Results 1 - 10 of 1,591 for were syndrome
  1. Roberts syndrome 
    Roberts syndrome is a genetic disorder characterized by limb and facial abnormalities. Affected individuals also grow slowly before and after birth. Mild to ...
    https://medlineplus.gov/genetics/condition/roberts-syndrome - Genetics
  2. Oral-facial-digital syndrome 
    Oral-facial-digital syndrome is actually a group of related conditions that affect the development of the oral cavity (the mouth and teeth), facial features, ...
    https://medlineplus.gov/.../condition/oral-facial-digital-syndrome - Genetics
  3. Alpha thalassemia X-linked intellectual disability syndrome 
    Alpha thalassemia X-linked intellectual disability syndrome is an inherited disorder that affects many parts of the body. This condition occurs almost exclusively ...
    https://medlineplus.gov/...x-linked-intellectual-disability-syndrome - Genetics
  4. 22q11.2 deletion syndrome 
    22q11.2 deletion syndrome (which is also known by several other names, listed below) is a disorder caused by the deletion of a small piece of chromosome 22. ...
    https://medlineplus.gov/genetics/condition/22q112-deletion-syndrome - Genetics
  5. DOORS syndrome 
    DOORS syndrome is a disorder involving multiple abnormalities that are present from birth (congenital). "DOORS" is an abbreviation for the major features of ...
    https://medlineplus.gov/genetics/condition/doors-syndrome - Genetics
  6. Joubert syndrome 
    Joubert syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even among members ...
    https://medlineplus.gov/genetics/condition/joubert-syndrome - Genetics
  7. Ehlers-Danlos syndrome 
    Ehlers-Danlos syndrome is a group of disorders that affect connective tissues supporting the skin, bones, blood vessels, and many other organs and tissues. ...
    https://medlineplus.gov/genetics/condition/ehlers-danlos-syndrome -
  8. 3MC syndrome 
    3MC syndrome is a disorder characterized by unusual facial features and problems affecting other tissues and organs.The distinctive facial features of people ...
    https://medlineplus.gov/genetics/condition/3mc-syndrome - Genetics
  9. Noonan syndrome 
    Noonan syndrome is a condition that affects many areas of the body. It is characterized by mildly unusual facial features, short stature, heart defects, bleeding ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  10. Ohdo syndrome, Say-Barber-Biesecker-Young-Simpson variant 
    The Say-Barber-Biesecker-Young-Simpson (SBBYS) variant of Ohdo syndrome is a rare condition characterized by genital abnormalities in males, missing or underdeveloped ...
    https://medlineplus.gov/...ay-barber-biesecker-young-simpson-variant - Genetics
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