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GENATLAS PHENOTYPE

last update : 25-10-2016

Symbol	FANCS
Location	17q21;31
Name	Fanconi anemia, complementation group S
Corresponding gene	BRCA1
Main clinical features	microcephaly, developmental delay, skin pigmentation and renal anomalis, with cellular sensitivity to chemotherapeutic agents increased susceptibility to cancer
Genetic determination	autosomal recessive
Function/system disorder	dermatology
	hematology
	osteo-articular
Type	disease

Remark(s)