Sitemap | Symptoma 16101 to 16200 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Lower Motor Neuron Syndrome with Late-Adult Onset Congenital Disorder of Glycosylation Type 1U Meningitis Muscular Dystrophy-Dystroglycanopathy Type A10 Charcot-Marie-Tooth Disease Type 2Q Congenital Non-Bullous Ichthyosiform Erythroderma ARCI 10 Primary Amebic Meningoencephalitis Nephrotic Syndrome Type 7 Idiopathic Basal Ganglia Calcification Type 4 Early Infantile Epileptic Encephalopathy Type 15 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Type 5 Amebic Cystitis Parasitic Intestinal Disease Joubert Syndrome Type 20 Pontocerebellar Hypoplasia Type 7 Congenital Leptin Deficiency Shigella Infection Acute Pericarditis Pontocerebellar Hypoplasia Type 8 Colonic Perforation Early Infantile Epileptic Encephalopathy Type 14 Colitis Combined Oxidative Phosphorylation Deficiency 15 Acute Gastroenteritis Autosomal Recessive Deafness 84B Combined Oxidative Phosphorylation Defect Type 13 Amebic Lung Abscess Amebic Liver Abscess Ectodermal Dysplasia Type 5 Hair Nail Traveler's Diarrhea Perrault Syndrome Type 2 Amebiasis Amblyopia Combined Oxidative Phosphorylation Defect Type 11 Catecholaminergic Polymorphic Ventricular Tachycardia Type 4 Leber Congenital Amaurosis Livedo Reticularis Hypogonadotropic Hypogonadism Type 16 Sinoatrial Node Dysfunction and Deafness Distal Spinal Muscular Atrophy Type 5 Hypogonadotropic Hypogonadism Type 15 Normal Pressure Hydrocephalus Usher Syndrome Type 1J Methylmalonic Acidemia with Homocystinuria Type cblJ Osteogenesis Imperfecta Type 13 Autosomal Recessive Primary Microcephaly Type 9 Seckel Syndrome Type 7 Hypogonadotropic Hypogonadism Type 12 Hypogonadotropic Hypogonadism Type 11 Hypogonadotropic Hypogonadism Type 10 Hypogonadotropic Hypogonadism Type 8 Amyotrophic Lateral Sclerosis Parkinson's Disease Muscular Dystrophy-Dystroglycanopathy Type A8 Autosomal Dominant Congenital Nystagmus 7 Cerebral Cortical Atrophy Joubert Syndrome Type 18 Adams-Oliver Syndrome Type 3 Extrapyramidal Disorder C3 Glomerulonephritis Alzheimer Disease Centronuclear Myopathy Type 4 Löffler Syndrome Extrinsic Allergic Alveolitis Distal Hereditary Motor Neuropathy Type 5B Mediastinal Emphysema Hyperphosphatasia with Mental Retardation Type 2 Alveolar Rupture Idiopathic Aplastic Anemia Extrapulmonary Alveolar Hypoventilation MEGDEL Syndrome Congenital Disorder of Glycosylation Type 2K Echinococcus Multilocularis Infection Common Variable Immunodeficiency Type 8 with Autoimmunity Parasite Decreased Lung Compliance Autosomal Recessive Congenital Cataract 5 Isolated Alar Cleft Pneumothorax Pontocerebellar Hypoplasia Type 1B Familial Hypertrophic Cardiomyopathy Type 21 Bronchioloalveolar Carcinoma Menstrual Cycle-Dependent Periodic Fever Autosomal Recessive Primary Microcephaly Type 8 Dilated Cardiomyopathy Type 2B Primary Coenzyme Q10 Deficiency Type 5 Primary Coenzyme Q10 Deficiency Type 3 Primary Coenzyme Q10 Deficiency Type 2 Primary Coenzyme Q10 Deficiency Type 6 Decreased Diffusion Capacity of the Lung Muscular Dystrophy-Dystroglycanopathy Type A7 Aluminum-Based Antacid Keratoconus 7 Alternating Exotropia Keratoconus 5 Alteplase UV-Sensitive Syndrome Type 2 Alstrom Syndrome Congenital Diarrhea Type 6 Joubert Syndrome Type 17
