Sitemap | Symptoma 15901 to 16000 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Age-Related Macular Degeneration 13 Familial Thoracic Aortic Aneurysm 8 Hodgkin Lymphoma Retinitis Pigmentosa with Situs Inversus 3q13.31 Microdeletion Syndrome Factor II Deficiency Specific Language Impairment 5 Myopia Type 22 Edema Nephrogenic Diabetes Insipidus Autosomal Recessive Primary Microcephaly Type 11 Nephrotic Syndrome Complex Cortical Dysplasia with other Brain Malformations Type 4 Acute Glomerulonephritis Complex Cortical Dysplasia with other Brain Malformations Type 3 Renal Vein Thrombosis Renal Amyloidosis Primary Amyloidosis Autonomic Neuropathy Familial Amyloid Polyneuropathy Multiple Congenital Anomalies - Hypotonia - Seizures Type 3 Meckel Syndrome Type 11 Hepatosplenic Amyloidosis Cutaneous Amyloidosis Nephronophthisis 16 Recessive Intermediate Charcot-Marie-Tooth Disease Type C Cone Rod Dystrophy Type 18 Secondary Amyloidosis Myeloma-associated Amyloidosis Childhood-Onset Epileptic Encephalopathy Amyloidosis in Familial Mediterranean Fever Fetal Akinesia - Cerebral and Retinal Hemorrhage Syndrome Restrictive Cardiomyopathy Estrogen Resistance Syndrome Bifascicular Block Left Anterior Fascicular Block Limb-Girdle Muscular Dystrophy Type 2S Muscular Dystrophy-Dystroglycanopathy Type B14 Muscular Dystrophy-Dystroglycanopathy Type A14 Left Ventricular Hypertrophy Ehlers-Danlos Syndrome Spondylodysplastic Type 2 Infiltrative Cardiomyopathy Central Precocious Puberty Type 2 Cardiac Amyloidosis Idiopathic Familial Pulmonary Arterial Hypertension Early Infantile Epileptic Encephalopathy Type 16 Acute Hemolytic Anemia Multiple Mitochondrial Dysfunctions Syndrome Type 3 Amprenavir Shaheen Syndrome Toxic Hemolytic Anemia Dowling-Degos Disease Type 1 Ampicillin-Sulbactam Perrault Syndrome Type 4 Adams-Oliver Syndrome Type 4 Hypersensitivity Myocarditis Distal Renal Tubular Acidosis Infantile Myofibromatosis Type 2 Muscular Dystrophy-Dystroglycanopathy Type A13 Unstable Angina Congenital Neutropenia - Myelofibrosis - Nephromegaly Syndrome Complex Cortical Dysplasia with other Brain Malformations Type 2 Bruxism Congenital Disorder of Deglycosylation Fanconi Anemia Complementation Group Q Hypomania Hypogonadotropic Hypogonadism Type 21 Hypogonadotropic Hypogonadism Type 20 Hypogonadotropic Hypogonadism Type 19 Cerebral Angiitis Hypogonadotropic Hypogonadism Type 18 Subarachnoid Hemorrhage Hypogonadotropic Hypogonadism Type 17 Malignant Hypertension Muscular Dystrophy-Dystroglycanopathy Type A12 Nephrotic Syndrome Type 8 Hypochromic Microcytic Anemia with Iron Overload Type 2 Drug-induced Cardiomyopathy ATP5A1-Related ATP Synthase Deficiency Postaxial Polydactyly Type A6 Xerostomia Osteogenesis Imperfecta Type 15 Oculocutaneous Albinism Type 7 Hypertensive Encephalopathy Heat Stroke Familial Episodic Pain Syndrome Type 1 Autosomal Recessive Monocyte and Dendritic Cell Deficiency Autosomal Dominant Aplasia and Myelodysplasia Perrault Syndrome 3 Delusion Complex Cortical Dysplasia with other Brain Malformations Type 1 Acute Amphetamine Intoxication Foveal Hypoplasia Type 2 Amphetamine Withdrawal Epileptic Encephalopathy Type Lennox-Gastaut Amphetamine Amphetamine Delusional Disorder Amyotrophic Lateral Sclerosis Type 21 Autosomal Dominant Cerebellar Ataxia - Deafness - Narcolepsy Stevens-Johnson Syndrome
