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Results 1 - 10 of 16 for Abnormal cerebral morphology
  1. Williams Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Genetic Disorders/Specifics ... Genetic Disorders ... Developmental Disabilities/Specifics ... Developmental Disabilities ... Genetic and Rare Diseases Information Center ...
  2. Huntington Disease From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Huntington's Disease/Learn More ... Huntington's Disease ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and ...
  3. Incontinentia Pigmenti From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Skin Pigmentation Disorders/Specifics ... Skin Pigmentation Disorders ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find ...
  4. Usher Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Usher Syndrome/Learn More ... Usher Syndrome ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information ...
  5. Dermatomyositis From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Myositis/Start Here ... Myositis ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information about ...
  6. Achondroplasia: About the Disease From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Dwarfism/Start Here ... Dwarfism ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health ... Find symptoms and other information about ...
  7. Alagille Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Bile Duct Diseases/Genetics ... Bile Duct Diseases ... Congenital Heart Defects/Genetics ... Congenital Heart Defects ... Genetic and Rare Diseases Information Center ... From ...
  8. ... Celia’s encephalopathy). This condition is characterized by abnormal brain function (encephalopathy) and intellectual disabilities that are apparent ...
  9. Campomelic dysplasia From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Birth Defects/Specifics ... Birth Defects ... Bone Diseases/Children ... Bone Diseases ... Genetic and Rare Diseases Information Center ... From the National Institutes of Health
  10. ... other nearby genes can cause seizures or other abnormal electrical activity in the brain. More About This Health Condition LETM1_HUMAN leucine zipper-EF-hand containing transmembrane protein 1 ... L, Scorrano L. LETM1, deleted in Wolf-Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability. Hum Mol Genet. 2008 Jan ...
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