• Subject ID is/contains
• Sex is (any) male female
• Age at echo is between 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 and 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 adult

(Multiple selections are allowed in the selection boxes below.)

Primary CHD phenotype	Secondary CHD phenotype	non-cardiac findings
(any) complex LVOTO non-obstructed LVOTO pure LVOTO	(any) cardiac situs cardiomyopathy conduction other vascular	(any) clinical genetic Dx connective tissue craniofacial cytogenic Dx developmental delay dysmorphic ear/nose/throat endocrine FTT (growth) gastrointestinal hematologic (blood) heterotaxy (visceral situs) immune abnormality metabolic multiple malformations muscular myopathy (skeletal) neurological ophthalmologic psychiatric pulmonary renal skeletal skin (dermatologic) urogenital vascular

Consanguinity	Teratogenic exposure
(any) denied No info available to date none reported other possible strong weak yes	(any) No info available to date none reported other possible strong weak yes
Family history of CHD	Family history, non-cardiac
(any) No info available to date none reported other possible strong weak yes	(any) cardiomyopathy No info available to date none reported other possible strong weak yes

Sort by Subject ID primary CHD sex age at echo height weight consanguinity teratogenic exposure family history of CHD family history, non-cardiac

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