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Results 1 - 7 of 7 for "Miller%syndrome"
  1. Miller syndrome is a rare condition that mainly affects the development of the face and limbs. The severity ...
  2. ... the DHODH gene have been found to cause Miller syndrome. Most of these mutations change single protein building ... mutations lead to the signs and symptoms of Miller syndrome. More About This Health Condition DHOdehase dihydroorotate dehydrogenase ...
  3. Learning about WAGR Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Eye Diseases/Genetics ... Eye Diseases ... Wilms Tumor/Genetics ... Wilms Tumor ... National Human Genome Research Institute ... From the National Institutes of Health ... WAGR syndrome ...
  4. Bone Diseases (National Library of Medicine)  
    Your bones help you move, give you shape and support your body. They are living tissues that rebuild constantly throughout your life. During childhood and ...
  5. Craniofacial Abnormalities (National Library of Medicine)  
    Craniofacial is a medical term that relates to the bones of the skull and face. Craniofacial abnormalities are birth defects of the face or head. Some, like cleft ...
  6. ... Hepatofacioneurocardiovertebral syndrome Paucity of interlobular bile ducts Watson-Miller syndrome Genetic Testing Registry: Alagille syndrome due to a ...
  7. Aniridia (American Association for Pediatric Ophthalmology and Strabismus)  
    GLOSSARY, TERMS, ACRONYMS, PHRASES, DEFINITIONS, DICTIONARY ... Shows a single glossary entry ... Eye Diseases/Specifics ... Eye Diseases ... American Association for Pediatric ...