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Results 1 - 10 of 1,551 for Clinical symptoms
  1. How Do Health Care Providers Diagnose Rett Syndrome? From the National Institutes of Health (Eunice Kennedy Shriver National Institute of Child Health and Human Development)  
    Rett Syndrome/Diagnosis and Tests ... Rett Syndrome ... Eunice Kennedy Shriver National Institute of Child Health and Human Development ... From the National Institutes ...
  2. Learning about Cri du Chat Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Developmental Disabilities/Specifics ... Developmental Disabilities ... National Human Genome Research Institute ... From the National Institutes of Health ... Cri du chat ...
  3. Learning about Gaucher Disease From the National Institutes of Health (National Human Genome Research Institute)  
    Gaucher disease is an autosomal recessive inherited disorder of metabolism where a type of fat (lipid) called glucocerebroside cannot be adequately degraded.
  4. Learning about Marfan Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Marfan Syndrome/Start Here ... Marfan Syndrome ... Marfan syndrome an inherited disorder of connective tissue occurring once in every 10,000 to 20,000 individuals.
  5. Congenital Central Hypoventilation Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Autonomic Nervous System Disorders/Specifics ... Autonomic Nervous System Disorders ... Genetic and Rare Diseases Information Center ... From the National Institutes ...
  6. HIV Medicines/Related Issues ... HIV Medicines ... Living with HIV/Related Issues ... Living with HIV ... COVID-19 (Coronavirus Disease 2019)/Related Issues ... COVID-19 (Coronavirus ...
  7. About Duchenne Muscular Dystrophy From the National Institutes of Health (National Human Genome Research Institute)  
    Muscular Dystrophy/Genetics ... Muscular Dystrophy ... National Human Genome Research Institute ... From the National Institutes of Health ... Duchenne muscular dystrophy ...
  8. Learning about Osteogenesis Imperfecta From the National Institutes of Health (National Human Genome Research Institute)  
    Osteogenesis Imperfecta/Genetics ... Osteogenesis Imperfecta ... Osteogenesis imperfecta is a genetic disorder that causes a person's bones to break easily, often ...
  9. Learning about Fragile X Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Fragile X syndrome is an inherited intellectual disability caused by a mutation in the FMR1 gene. ... Fragile X Syndrome/Start Here ... Fragile X Syndrome ... National ...
  10. About Myotonic Dystrophy From the National Institutes of Health (National Human Genome Research Institute)  
    Myotonic dystrophy is an inherited type of muscular dystrophy that affects the muscles and other body systems. ... Muscular Dystrophy/Genetics ... Muscular Dystrophy
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