Griscelli Syndrome, Type 1,Diarrhea 2, With Microvillus Atrophy,Congenital Diarrhea,Griscelli Syndrome

Ventricular Septal Defect,Muscular Disease,Heart Disease,Lymphopenia,Congenital Fiber-Type Disproportion,Mitral Valve Insufficiency,Severe Combined Immunodeficiency,Aortic Valve Disease 2,Congenital Structural Myopathy,Myopathy,Cardiomyopathy, Dilated, 1e,Myofibrillar Myopathy,Atrial Heart Septal Defect,Mitochondrial Dna Depletion Syndrome 12b,Muscle Tissue Disease,Neuromuscular Disease,Myopathy, Myosin Storage, Autosomal Dominant,Bethlem Myopathy 1,Hypertrophic Cardiomyopathy,Myosinopathies,Familial Isolated Dilated Cardiomyopathy,Rasopathy,Autosomal Dominant Distal Myopathy,Myocardial Infarction,Myopathy, Distal, 1,Muscular Dystrophy,Progressive Familial Heart Block,Tibial Muscular Dystrophy,Hyaline Body Myopathy,Atrial Standstill 1,Combined Immunodeficiency,Dilated Cardiomyopathy,Oculopharyngeal Muscular Dystrophy,Combined T And B Cell Immunodeficiency,Long Qt Syndrome,Malignant Hyperthermia,Heart Conduction Disease,Muscular Dystrophy, Congenital, Lmna-Related,Ebstein Anomaly,Cardiac Conduction Defect,Cardiomyopathy, Familial Hypertrophic, 4,Congestive Heart Failure,Endocardial Fibroelastosis,Rigid Spine Muscular Dystrophy 1,Camptocormism,Noonan Syndrome With Multiple Lentigines,Respiratory Failure,Mobitz Type Ii Atrioventricular Block,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Long Qt Syndrome 2,Danon Disease,Congenital Myasthenic Syndrome,Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, With Or Without Atrial Dysfunction And/Or Dilated Cardiomyopathy,Scapuloperoneal Myopathy, Myh7-Related,Restrictive Cardiomyopathy,Arrhythmogenic Right Ventricular Cardiomyopathy,Brugada Syndrome,Stormorken Syndrome,Immune Deficiency Disease,Familial Atrial Fibrillation,Atrioventricular Block,First-Degree Atrioventricular Block,Tricuspid Valve Disease,Barth Syndrome,Holt-Oram Syndrome,Long Qt Syndrome 1,Cardiomyopathy, Familial Hypertrophic, 1,Wolff-Parkinson-White Syndrome,Intrinsic Cardiomyopathy,Peripartum Cardiomyopathy,Lipoprotein Quantitative Trait Locus,Atrial Fibrillation,Scapuloperoneal Myopathy,Cardiac Arrest,Left Ventricular Noncompaction,Myopathy, Myosin Storage, Autosomal Recessive,Catecholaminergic Polymorphic Ventricular Tachycardia,Batten-Turner Congenital Myopathy,Myopathy, Congenital, With Fiber-Type Disproportion,Miyoshi Muscular Dystrophy,Craniosynostosis 4,Cardiomyopathy, Dilated, 1b

Chondrocalcinosis,Usher Syndrome, Type I,Anterior Segment Dysgenesis 5,Usher Syndrome

Amebiasis,Myopathy, Centronuclear, 1,Deafness, Autosomal Recessive 12,Chromosome 17p13.3, Centromeric, Duplication Syndrome,Usher Syndrome, Type I,Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna,Sclerosing Keratitis,Usher Syndrome,Miller-Dieker Lissencephaly Syndrome,Deafness, Autosomal Dominant 48