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- How Do Health Care Providers Diagnose Rett Syndrome? (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 ...
- Learning about Cri du Chat Syndrome (National Human Genome Research Institute)Developmental Disabilities/Specifics ... Developmental Disabilities ... National Human Genome Research Institute ... From the National Institutes of Health ... Cri du chat ...
- Learning about Gaucher Disease (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.
- Learning about Marfan Syndrome (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.
- Congenital Central Hypoventilation Syndrome (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 ...
- COVID-19 and Special Considerations in People with HIV (National Institutes of Health)HIV Medicines/Related Issues ... HIV Medicines ... Living with HIV/Related Issues ... Living with HIV ... COVID-19 (Coronavirus Disease 2019)/Related Issues ... COVID-19 (Coronavirus ...
- About Duchenne Muscular Dystrophy (National Human Genome Research Institute)Muscular Dystrophy/Genetics ... Muscular Dystrophy ... National Human Genome Research Institute ... From the National Institutes of Health ... Duchenne muscular dystrophy ...
- Learning about Osteogenesis Imperfecta (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 ...
- Learning about Fragile X Syndrome (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 ...
- About Myotonic Dystrophy (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