16101 to 16200 most common queries

List represents a sample of symptoms, diseases, and other queries. Updated weekly.

• Hemiplegia
• 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