16401 to 16500 most common queries

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

• Hydatidiform Mole 2
• Hereditary Factor XIIIA Deficiency
• Congenital Malformation
• High Myopia - Cataract - Vitreoretinal Degeneration
• Chronic Nephritis
• Toxic Amblyopia
• Stickler Syndrome Type 5
• Acute Intermittent Porphyria
• Arthrogryposis, Perthes Disease and Upward Gaze Palsy
• Chronic Thromboembolic Pulmonary Hypertension
• Gastritis
• Peptic Esophagitis
• Hyperlipoproteinemia Type 4
• Migraine
• Disulfiram-like Reaction
• Cryopyrin-Associated Periodic Syndrome
• Premenstrual Syndrome
• Failure of Lid Closure
• Alcoholic Cerebellar Degeneration
• Charcot-Marie-Tooth Disease Type 2O
• Extruded Intervertebral Disc
• Diabetes Insipidus
• Familial Juvenile Hyperuricemic Nephropathy Type 3
• Submandibular Duct Calculus
• Ciguatera Poisoning
• Consumption of Red Wine
• Familial Retinal Arterial Macroaneurysm
• Acromioclavicular Separation
• Warburg Micro Syndrome 3
• Spinal Cord Tumor of Foramen Magnum
• Nocturnal Leg Cramp
• Adams-Oliver Syndrome Type 2
• Vitamin B12 Deficiency Anemia
• Hereditary Sensory and Autonomic Neuropathy Type 2C
• Hyperphosphatasia with Mental Retardation Type 3
• T-Cell Acute Lymphoblastic Leukemia
• 3M Syndrome Type 3
• Hereditary Late-Onset Parkinson Disease Type 17
• Autosomal Recessive Mental Retardation Type 15
• Glycoprotein 6 Deficiency
• Glycoprotein 1A Deficiency
• Restless Legs Syndrome
• Nephrotic Syndrome Type 6
• Cardiac Asthma
• Leber Congenital Amaurosis Type 16
• Alcoholic Neuropathy
• Geleophysic Dysplasia 2
• Severe Aplastic Anemia
• Retinitis Pigmentosa 62
• Alcoholic Myopathy
• Meckel Syndrome Type 10
• AMACR Deficiency
• Joubert Syndrome Type 13
• Monocytopenia with Susceptibility to Infections
• Hermansky-Pudlak Syndrome Type 9
• Brittle Cornea Syndrome Type 2
• Upper Urinary Tract Infection
• Myopia Type 21
• Aortic Aneurysm and Dissection
• Tracheal Carcinoma
• Immunodeficiency Type 31C
• Autosomal Recessive Nail Dysplasia
• Episodic Ataxia
• Hypomagnesemia
• Hyperbiliverdinemia
• Diabetic Ketotic Coma
• Autosomal Dominant Deafness 64
• Hyperuricemia
• Atrial Flutter
• Focal Segmental Glomerulosclerosis Type 6
• Hereditary Sensory and Autonomic Neuropathy Type 1E
• Bacterial Otitis Media
• Kappa Chain Deficiency
• Invasive Candidiasis
• Hydrophobia
• Acute Alcohol Intoxication
• Limbal Stem Cell Deficiency
• Chronic Kidney Disease
• Multiple Congenital Anomalies - Hypotonia - Seizures Type 1
• Fecal Incontinence
• Myoclonic Jerking
• Chondrodysplasia with Joint Dislocations Type gPAPP
• Hermansky-Pudlak Syndrome Type 7
• Sleep Deprivation
• Alcohol-induced Hypoglycemia
• Autosomal Recessive Spastic Paraplegia Type 52
• Autosomal Recessive Spastic Paraplegia Type 47
• Intracranial Neoplasm
• Distal Myopathy Type 4
• Post-Polycythemia Vera Myelofibrosis
• Paranoid Personality Disorder
• TMEM70-Related Mitochondrial Encephalo-Cardio-Myopathy
• Familial Atrial Fibrillation Type 12
• Enthesitis-Related Arthritis
• Familial Atrial Fibrillation 11
• Atypical Pneumonia
• Alcohol Hallucinosis
• Late-onset Depression
• Acute Gastritis
• Hypotonia-Failure to Thrive-Microcephaly Syndrome