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Results 1 - 10 of 16 for "Congenital%hearts%disease"
  1. Critical congenital heart disease 
    Critical congenital heart disease (CCHD) is a term that refers to a group of serious heart defects that are present from birth. These abnormalities result from ...
    https://medlineplus.gov/.../critical-congenital-heart-disease - Genetics
  2. McKusick-Kaufman syndrome 
    ... DC. Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein. PLoS ...
    https://medlineplus.gov/genetics/condition/mckusick-kaufman-syndrome - Genetics
  3. NOTCH1 gene 
    ... Condition NOTCH1 gene mutations are involved in critical congenital heart disease. Individuals with this condition have one or more ...
    https://medlineplus.gov/genetics/gene/notch1 - Genetics
  4. JAG1 gene 
    ... Health Condition MedlinePlus Genetics provides information about Critical congenital heart disease More About This Health Condition Increased activity (expression) ...
    https://medlineplus.gov/genetics/gene/jag1 - Genetics
  5. GJA1 gene 
    ... Health Condition MedlinePlus Genetics provides information about Critical congenital heart disease More About This Health Condition MedlinePlus Genetics provides ...
    https://medlineplus.gov/genetics/gene/gja1 - Genetics
  6. TBX5 gene 
    ... PubMed Mori AD, Bruneau BG. TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed. Curr Opin Cardiol. 2004 ...
    https://medlineplus.gov/genetics/gene/tbx5 - Genetics
  7. Primary ciliary dyskinesia 
    ... Morillas HN, Noone PG, Zariwala MA, Knowles MR. Congenital heart disease and other heterotaxic defects in a large cohort ...
    https://medlineplus.gov/.../condition/primary-ciliary-dyskinesia - Genetics
  8. Cri-du-chat syndrome 
    ... J, Schimmenti L. Cri du chat syndrome and congenital heart disease: a review of previously reported cases and presentation ...
    https://medlineplus.gov/genetics/condition/cri-du-chat-syndrome - Genetics
  9. MKKS gene 
    ... DC. Nuclear/cytoplasmic transport defects in BBS6 underlie congenital heart disease through perturbation of a chromatin remodeling protein. PLoS ...
    https://medlineplus.gov/genetics/gene/mkks - Genetics
  10. Holt-Oram syndrome 
    ... PubMed Mori AD, Bruneau BG. TBX5 mutations and congenital heart disease: Holt-Oram syndrome revealed. Curr Opin Cardiol. 2004 ...
    https://medlineplus.gov/genetics/condition/holt-oram-syndrome - Genetics
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