Focal Dermal Hypoplasia

MeSH code information
  • Name
  • Concept
    Scope note:A genetic skin disease characterized by hypoplasia of the dermis, herniations of fat, and hand anomalies. It is found exclusively in females and transmitted as an X-linked dominant trait.
  • Tree numbers
    • C05.116.099.370.380
    • C16.131.077.350.424
    • C16.131.831.350.424
    • C16.320.322.186
    • C16.320.850.250.424
    • C17.800.804.350.424
    • C17.800.827.250.424
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