bn:04746692n
Noun Named Entity
Categories: Congenital disorders
EN
Char syndrome  Char  Patent Ductus Arteriosus With Facial Dysmorphism and Abnormal Fifth Digits
EN
Char syndrome is an autosomal dominant congenital disease caused by mutations in TFAP2B gene which affects the development of the bones of the face as well as the heart and limbs. Wikipedia
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EN
Char syndrome is an autosomal dominant congenital disease caused by mutations in TFAP2B gene which affects the development of the bones of the face as well as the heart and limbs. Wikipedia
Patent ductus arteriosus with facial dysmorphism and abnormal fifth digits Wikidata