Congenital heart defects, multiple types, 2

MONDO:0014000

Any congenital heart disease characterized by variable features including polyvalvular heart disease, growth failure, joint hypermobility, hypotonia, and hearing loss due to a variation in the TAB2 gene.

Also known as: TAB2 congenital heart malformation, TAB2-related syndromic congenital heart disease, congenital heart defects, multiple types, 2, congenital heart malformation caused by mutation in TAB2, CHTD2

76 clinical trials for this condition and its sub-types, 0 tagged with Congenital heart defects, multiple types, 2 itself.

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↑ Cardiogenetic disease (618) ↑ Congenital heart malformation (155) ↑ Congenital heart defects, multiple types (0)

Including sub-types (76) Tagged with Congenital heart defects, multiple types, 2 (0)

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