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Results 1 - 10 of 14 for Hereditary cardiac anomaly
  1. Coronary Artery Anomalies (Texas Heart Institute)  
    A coronary artery anomaly (CAA) is a defect in one or more of the coronary arteries of the heart. The defect is congenital (present at birth). CAAs may ...
  2. ... radiologist, sclerotherapy, embolization, blood vessels, angiogram, Cobb syndrome, hereditary hemorrhagic telangiectasia, Parkes Weber syndrome, Wyburn-Mason syndrome, Bonnet-Dechaume-Blanc syndrome, AVMs of the retina, AVMs in the head, AVMs in the skull, vascular anomaly, vascular malformations
  3. Alagille Syndrome From the National Institutes of Health (Genetic and Rare Diseases Information Center)  
    Congenital Heart Defects/Genetics ... Congenital Heart Defects ... Bile Duct Diseases/Genetics ... Bile Duct Diseases ... Genetic and Rare Diseases Information Center ... From ...
  4. Learning about Velocardiofacial Syndrome From the National Institutes of Health (National Human Genome Research Institute)  
    Parathyroid Disorders/Genetics ... Parathyroid Disorders ... Cleft Lip and Palate/Specifics ... Cleft Lip and Palate ... Congenital Heart Defects/Specifics ... Congenital Heart ...
  5. ... paradoxical venous embolism) Infection in the brain or heart valve, especially in patients with HHT ... Prabhudesai V, Faughnan ME. Pulmonary vascular anomalies. In: ... DL, Tomaselli GF, Bhatt DL, Solomon SD, eds. Braunwald's Heart ...
  6. Talking Glossary of Genetic Terms From the National Institutes of Health (National Human Genome Research Institute)  
    Genetic Disorders/Reference Desk ... Genetic Disorders ... Genes and Gene Therapy/Reference Desk ... Genes and Gene Therapy ... Genetic Testing/Reference Desk ... Genetic Testing
  7. Arteriovenous Malformation (AVMs) From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Arteriovenous Malformations/Start Here ... Arteriovenous Malformations ... Fistulas/Specifics ... Fistulas ... National Institute of Neurological Disorders and Stroke ... From ...
  8. ... mutation during malignant progression in a patient with hereditary multiple osteochondromas. Cancer Genet. 2015 Mar;208(3): ... splice mutation and mRNA decay of EXT2 provoke hereditary multiple exostoses. PLoS One. 2014 Apr 11;9( ...
  9. 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 ...
  10. Kearns-Sayre Syndrome From the National Institutes of Health (National Center for Advancing Translational Sciences)  
    Neuromuscular Disorders/Specifics ... Neuromuscular Disorders ... Eye Diseases/Specifics ... Eye Diseases ... National Center for Advancing Translational Sciences ... From the ...
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