Focal Dermal Hypoplasia
MeSH code information
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Name
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ConceptScope 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.
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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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Qualifiersdiagnosis, 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