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    1. A full term girl

      Case1: gestational age 40 weeks female

      DiseaseAssertion: Poor feeding, cyanosis, and difficulty with breathing.

      FamilyInfo: Healthy non‐consanguineous parents. Echocardiographic in the mother and sister were normal. Father had mild dilatation of the left atrium with an abnormal flow pattern in the mitral valve, otherwise healthy.

      ParentalTesting: c.2373_2374insG mutation found in the mother

      CasePresentingHPOs:HP:0025169,

      CaseHPOFreeText: hypertrophic non‐obstructive cardiomyopathy with poor left and right ventricular systolic function. The left ventricular end diastolic diameter measured 17.3 mm (99% of normal), end systolic diameter 12.9 mm (116% of normal), and left ventricular posterior wall 3.6 mm (111% of normal). The intraventricular septum measured 11.8 mm (288% of normal). The shortening fraction of the left ventricle was decreased to 25%. Multiple abnormal small communications with a minimal flow between a coronary artery and the right ventricle were observed in the apical portion of the interventricular septum. There were no structural congenital heart defects.

      CaseNotHPOs: NR

      CaseNotHPOFreeText: NR

      CasePreviousTesting: NR

      Genotyping Method:

      FunctionalAnalysis: NR

      Variant: NM_006073.4(TRDN):c.1624+1G>A

      ClinVar:2152664

      CAID: CA147231745

      gnomAD:NR

      AdditionalInfo:NR