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Results 1 - 1 of 1 for "Child%syndrome"
  1. NSDHL gene 
    ... congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD syndrome). Most of these mutations change single protein building ... cholesterol synthesis leads to the specific features of CHILD syndrome. More About This Health Condition H105E3 NSDHL_HUMAN ...
    https://medlineplus.gov/genetics/gene/nsdhl - Genetics