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
  • Qualifiers
    diagnosis, parasitology, immunology, microbiology, diagnostic imaging, physiopathology, rehabilitation, enzymology, etiology, mortality, epidemiology, blood, cerebrospinal fluid, chemically induced, diet therapy, drug therapy, therapy, psychology, urine, virology, veterinary, history, classification, economics, embryology, genetics, nursing, radiotherapy, ethnology, prevention & control, pathology, metabolism, complications, surgery
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