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Boli A-Z Aarskog-Scott Syndrome Acid-Labile Subunit Deficiency Acrocallosal Syndrome Acrodermatitis Enteropathica, Zinc-Deficiency Type Acromegaly Acrorenal-Mandibular Syndrome Acute Myocardial Infarction Acute Pancreatitis Adenoma Adrenal Adenoma Aging Alport Syndrome, X-Linked Al-Raqad Syndrome Amelogenesis Imperfecta Amyloidosis Androgen Insensitivity Syndrome, Mild Aneurysm Aneurysm of Sinus of Valsalva Angel-Shaped Phalangoepiphyseal Dysplasia Angiomyolipoma Aniridia 1 Anorexia Nervosa 1 Aortic Aneurysm Aortitis Arachnoid Cysts Arachnoiditis Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atrial Septal Aneurysm Autonomic Dysfunction Autosomal Dominant Polycystic Kidney Disease Autosomal Genetic Disease Bardet-Biedl Syndrome Bile Duct Cysts Blastoma Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Brittle Bone Disorder Bronchiectasis Budd-Chiari Syndrome Caroli Disease Carotid Artery Dissection Central Nervous System Lymphoma Cerebellofaciodental Syndrome Cerebral Aneurysms Cerebritis Cholangitis Cholera Cholestasis Chromophobe Renal Cell Carcinoma Chronic Diarrhea Due to Glucoamylase Deficiency Chronic Pain Ciliopathy Cleft Lip Collecting Duct Carcinoma Complement Factor D Deficiency Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy Congenital Hepatic Fibrosis Congenital Hypothyroidism Corneal Dystrophy Corneal Dystrophy, Fleck Coronary Aneurysm Coronary Artery Dissection, Spontaneous Cortical Blindness Crescentic Glomerulonephritis Cystadenoma Cystic Fibrosis Cystic Kidney Disease Cystic Nephroma Cystinuria Dementia Dermal Ridges-off-the-End Dextrocardia Diabetes Insipidus Diabetes Mellitus Diastolic Heart Failure Differentiated Thyroid Carcinoma Diffuse Lymphatic Malformation Dihydropyrimidinase Deficiency Dimethylglycine Dehydrogenase Deficiency Diverticulitis Duodenal Obstruction Duodenitis Encephalocele Endotheliitis End Stage Renal Failure Eosinophilic Fasciitis Epidermolysis Bullosa Epidermolysis Bullosa Junctionalis with Pyloric Atresia Epidermolysis Bullosa with Pyloric Atresia Episodic Kinesigenic Dyskinesia 1 Factor Xiii Deficiency Familial Adenomatous Polyposis 1 Fibrous Histiocytoma Focal Segmental Glomerulosclerosis Fructosuria, Essential Germ Cells Tumors Gianotti Crosti Syndrome Glioma Glomerulonephritis Hajdu-Cheney Syndrome Headache Helix Syndrome Hemophagocytic Lymphohistiocytosis, Familial, 1 Hepatic Adenomas, Familial Hepatitis Hepatoblastoma Histiocytoma Holoprosencephaly Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hyperinsulinemic Hypoglycemia Hyperinsulinism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertensive Heart Disease Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 Hypertrophic Pyloric Stenosis Hypoglycemia Hypokalemia Hypoparathyroidism, Sensorineural Deafness, and Renal Disease Hypophosphatemia Hypouricemia, Renal, 1 Hypoxia Ichthyosis Vulgaris Immunoglobulin E Concentration, Serum Infertility Insulin-Like Growth Factor I Interstitial Nephritis Intracranial Aneurysm Intracranial Cysts Intracranial Hypotension Isolated Optic Neuritis Junctional Epidermolysis Bullosa Juvenile Hereditary Hemochromatosis Kartagener Syndrome Kidney Disease Lattice Corneal Dystrophy Left Ventricular Noncompaction Liver Disease Lymphangioleiomyomatosis Lymphangiomatosis Lymphatic Malformations Lymphocele Lymphoma Male Infertility Malignant Hypertension Marfan Syndrome Medullary Sponge Kidney Melanoma Membranous Nephropathy Meningioma, Familial Mn1 Mucolipidosis Iii Alpha/beta Mucolipidosis Iii Gamma Multicystic Dysplastic Kidney Muscular Dystrophy, Duchenne Type Myocardial Infarction Myopathy, Spheroid Body Nephrocalcinosis Nephrolithiasis Nephrolithiasis, X-Linked Recessive, with Renal Failure Nephronophthisis Nephrotic Syndrome Neurofibroma Neuronitis Occult Macular Dystrophy Orbital Cyst Orofaciodigital Syndrome Orofaciodigital Syndrome I Osteogenesis Imperfecta, Type I Osteomalacia Ovarian Cyst Pachyonychia Congenita 2 Pancreatitis Pancreatitis, Hereditary Papillary Adenoma Pericardial Effusion Pericarditis Peritonitis Pineal Cyst Pituitary Adenoma Pleuropulmonary Blastoma Polycystic Kidney Disease 1 Polycystic Kidney Disease 2 Polycystic Kidney Disease 3 Polycystic Kidney Disease 4 with or Without Hepatic Disease Polycystic Kidney Disease 5 Polycystic Liver Disease Polycystic Liver Disease 1 Polycythemia Polymyositis Portal Hypertension Premature Chromatid Separation Trait Priapism Primary Effusion Lymphoma Primary Hyperoxaluria Proliferative Glomerulonephritis Prostatic Cyst Prostatitis Psoriasis Psoriasis 13 Pulmonary Edema Pyelonephritis Pyloric Atresia Pyloric Stenosis Pyruvate Kinase Deficiency of Red Cells Pyuria Radin Blood Group Antigen Rapidly Progressive Glomerulonephritis Recurrent Acute Pancreatitis Renal Dysplasia, Cystic Renal Hypertension Renal Osteodystrophy Renal Pelvis Squamous Cell Carcinoma Renal Tuberculosis Restrictive Dermopathy, Lethal Reticular Dysgenesis Retinal Degeneration Retinal Detachment Retinitis Retinitis Pigmentosa Rhombencephalosynapsis Sarcoidosis 2 Sclerosteosis 1 Situs Inversus Sotos Syndrome 1 Spastic Ataxia, Charlevoix-Saguenay Type Spontaneous Intracranial Hypotension Squamous Cell Carcinoma Steatocystoma Multiplex Sturge-Weber Syndrome Subdural Empyema Sveinsson Chorioretinal Atrophy Testicular Germ Cell Tumor Testicular Germ Cell Tumor 1 Tetraamelia Syndrome, Autosomal Recessive Thalassemia Thrombosis Thyroiditis Tuberous Sclerosis Tuberous Sclerosis 2 Umbilical Hernia Undifferentiated Embryonal Sarcoma of the Liver Unilateral Multicystic Dysplastic Kidney Ureterocele Usher Syndrome Usher Syndrome, Type Ic Weber Syndrome Wilson Disease Xanthogranulomatous Pyelonephritis