BabelNet

bn:04746692n

Noun Named Entity

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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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IS A

γενετικό ελάττωμα

σπάνια πάθηση

ανοικτός αρτηριακός πόρος

πτώση

GENETIC ASSOCIATION

TFAP2B

HEALTH SPECIALTY

Ιατρική γενετική