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Results 1 - 4 of 4 for Congenital heart disease variable
  1. Heterotaxy syndrome 
    ... most serious complications are generally caused by critical congenital heart disease, a group of complex heart defects that are ... particular genetic mutation; this situation is known as variable ... isolated congenital heart defects in some family members and heterotaxy ...
    https://medlineplus.gov/genetics/condition/heterotaxy-syndrome - Genetics
  2. 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
  3. Spinal muscular atrophy 
    ... with spinal muscular atrophy type 0 also have heart defects that are present from birth (congenital).Spinal muscular atrophy type I (also called Werdnig-Hoffmann disease) is the most common form of the condition. ...
    https://medlineplus.gov/genetics/condition/spinal-muscular-atrophy - Genetics
  4. Hereditary sensory and autonomic neuropathy type II 
    ... HSAN2 on the autonomic nervous system are more variable. Some infants with HSAN2 have digestive problems such ... not show signs and symptoms of the condition. Congenital sensory neuropathy Hereditary sensory and autonomic neuropathy type ...
    https://medlineplus.gov/...-sensory-and-autonomic-neuropathy-type-ii - Genetics