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Results 51 - 60 of 104 for Congenital heart anomalies
  1. Hereditary hemochromatosis 
    ... arthritis, liver disease (cirrhosis) or liver cancer, diabetes, heart abnormalities, or skin discoloration. The appearance and severity of ...
    https://medlineplus.gov/.../condition/hereditary-hemochromatosis - Genetics
  2. Chylomicron retention disease 
    ... ability to sense vibrations. Rarely, affected individuals have heart abnormalities or muscle wasting (amyotrophy). Chylomicron retention disease is ...
    https://medlineplus.gov/.../condition/chylomicron-retention-disease - Genetics
  3. Abdominal wall defect 
    ... frequently have multiple birth defects, such as a congenital heart defect. Additionally, underdevelopment of the lungs is often ...
    https://medlineplus.gov/genetics/condition/abdominal-wall-defect - Genetics
  4. Noonan syndrome 
    ... with Noonan syndrome have some form of critical congenital heart disease. The most common heart defect in these ...
    https://medlineplus.gov/genetics/condition/noonan-syndrome - Genetics
  5. Cri-du-chat syndrome 
    ... J, Schimmenti L. Cri du chat syndrome and congenital heart disease: a review of previously reported cases and ...
    https://medlineplus.gov/genetics/condition/cri-du-chat-syndrome - Genetics
  6. FG syndrome 
    ... Stevenson RE. FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for ...
    https://medlineplus.gov/genetics/condition/fg-syndrome - Genetics
  7. MTHFR gene 
    ... Q. 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review. Am J Epidemiol. 2000 May ...
    https://medlineplus.gov/genetics/gene/mthfr - Genetics
  8. Smith-Lemli-Opitz syndrome 
    ... FD. RSH/Smith-Lemli-Opitz syndrome: a multiple congenital anomaly/mental retardation syndrome due to an inborn error ...
    https://medlineplus.gov/.../condition/smith-lemli-opitz-syndrome - Genetics
  9. X-linked chondrodysplasia punctata 2 
    ... JC, Rope AF. A novel X-linked multiple congenital anomaly syndrome associated with an EBP mutation. Am J ...
    https://medlineplus.gov/.../x-linked-chondrodysplasia-punctata-2 - Genetics
  10. EBP gene 
    ... JC, Rope AF. A novel X-linked multiple congenital anomaly syndrome associated with an EBP mutation. Am J ...
    https://medlineplus.gov/genetics/gene/ebp - Genetics
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