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GENATLAS PHENOTYPE

last update : 15-12-2012

Symbol	FFDD4
Location	10q23.33
Name	focal facial dermal dysplasia 4
Corresponding gene	CYP26C1
Main clinical features	developmental defects characterized by bitemporal or preauricular skin lesions resembling aplasia cutis congenita, isolated
Genetic determination	autosomal recessive
Function/system disorder	dermatology
Type	disease

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