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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