Vezi şi

Boli A-Z Acute Dacryocystitis Adie Pupil Aging Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Atrial Standstill 1 Autosomal Dominant Limb-Girdle Muscular Dystrophy Bethlem Myopathy 1 Blood Group--Ahonen Cardiomyopathy, Dilated, 1b Cardiomyopathy, Dilated, 1bb Cardiomyopathy, Dilated, 1cc Cardiomyopathy, Dilated, 1d Cardiomyopathy, Dilated, 1dd Cardiomyopathy, Dilated, 1e Cardiomyopathy, Dilated, 1ee Cardiomyopathy, Dilated, 1ff Cardiomyopathy, Dilated, 1g Cardiomyopathy, Dilated, 1gg Cardiomyopathy, Dilated, 1h Cardiomyopathy, Dilated, 1hh Cardiomyopathy, Dilated, 1i Cardiomyopathy, Dilated, 1ii Cardiomyopathy, Dilated, 1j Cardiomyopathy, Dilated, 1jj Cardiomyopathy, Dilated, 1k Cardiomyopathy, Dilated, 1kk Cardiomyopathy, Dilated, 1l Cardiomyopathy, Dilated, 1m Cardiomyopathy, Dilated, 1nn Cardiomyopathy, Dilated, 1o Cardiomyopathy, Dilated, 1p Cardiomyopathy, Dilated, 1q Cardiomyopathy, Dilated, 1r Cardiomyopathy, Dilated, 1u Cardiomyopathy, Dilated, 1v Cardiomyopathy, Dilated, 1w Cardiomyopathy, Dilated, 1x Cardiomyopathy, Dilated, 1z Cardiomyopathy, Dilated, 2a Cardiomyopathy, Dilated, 2b Cardiomyopathy, Dilated, 3b Cardiomyopathy Due to Anthracyclines Catecholaminergic Polymorphic Ventricular Tachycardia Clear Cell Acanthoma Congenital Fiber-Type Disproportion Congestive Heart Failure Craniometaphyseal Dysplasia, Autosomal Dominant Deafness, Autosomal Dominant 2a Deafness, Autosomal Recessive 44 Dilated Cardiomyopathy Dilated Cardiomyopathy 1t Dystonia 24 Emerinopathy Emery-Dreifuss Muscular Dystrophy Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant External Ear Disease Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form Familial Partial Lipodystrophy Gestational Choriocarcinoma Hepatic Adenomas, Familial Leber Congenital Amaurosis 2 Long Qt Syndrome 1 Long Qt Syndrome 15 Muscle Eye Brain Disease Muscle Tissue Disease Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Congenital, 1b Muscular Dystrophy, Congenital, Lmna-Related Muscular Dystrophy, Congenital Merosin-Deficient, 1a Muscular Dystrophy, Duchenne Type Muscular Dystrophy-Dystroglycanopathy , Type a, 4 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 Muscular Dystrophy-Dystroglycanopathy , Type B, 6 Muscular Dystrophy, Limb-Girdle, Type 1b Muscular Dystrophy, Limb-Girdle, Type 2c Myofibrillar Myopathy Myopathy, Myofibrillar, 2 Myopathy, Proximal, and Ophthalmoplegia Myopathy, X-Linked, with Excessive Autophagy Otitis Externa Otomycosis Pelger-Huet Anomaly Primary Cutaneous Amyloidosis Primary Systemic Mycosis Spontaneous Ocular Nystagmus Sporotrichosis Triosephosphate Isomerase Deficiency Ullrich Congenital Muscular Dystrophy 1 Walker-Warburg Syndrome