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

Ehlers-Danlos Syndrome Kyphoscoliotic Type 2 Chromosome 16q22 Deletion Syndrome Dilated Cardiomyopathy Folic Acid Deficiency Familial Congenital Mirror Movements 2 Wernicke-Korsakoff Syndrome Testicular Atrophy Congenital Disorder of Glycosylation Type 1R Usher Syndrome Type 3B Psychomotor Retardation - Epilepsy and Craniofacial Dysmorphism Cone Rod Dystrophy Type 16 Lethal Neonatal Spasticity - Epileptic Encephalopathy Chronic Anxiety Pulmonary Tuberculosis Atrial Fibrillation Retinitis pigmentosa 63 Alcohol Dementia Early-Onset Spastic Ataxia - Neuropathy Syndrome Septic Arthritis Portal Hypertension Secondary Cardiomyopathy Congenital Cataract-Hearing Loss-Severe Developmental Delay Syndrome Cardiac Beriberi Transient Infantile Hypertriglyceridemia and Hepatosteatosis Atrial Septal Defect 9 Dupuytren Contracture Scurvy Familial Cold Autoinflammatory Syndrome Type 3 Bacterial Meningitis Joubert Syndrome Type 16 Alcoholic Cardiomyopathy Joubert Syndrome Type 15 Bleeding Peptic Ulcer Encephalopathy Episodic due to Thiamine Pyrophosphokinase Deficiency Hyperlipidemia Type 5 Dominant Intermediate Charcot-Marie-Tooth Disease Type E Tuberculosis Gout Congenital Non-Goitrous Hypothyroidism Type 6 Pachydermoperiostosis Type 2 Esophageal Varices on Barium Swallow Marchiafava Bignami Disease Autosomal Recessive Cutis Laxa Type 1B Atrial Arrhythmia Charcot-Marie-Tooth Disease Type 2P Water Soluble Vitamin Deficiency Vitamin B6 Deficiency Joubert Syndrome Type 14 Haemophilus Influenzae Pneumonia Congenital Cerulean Cataract Type 5 Carcinoma of the Larynx Pharyngeal Carcinoma Familial Febrile Seizures Type 11 Pellagra Familial Temporal Lobe Epilepsy Type 5 Xeroderma Chronic Alcoholism Magnesium Deficiency Fatty Liver Portal Cirrhosis Hemorrhoids Nephronophthisis 13 Alcoholic Hepatitis Pulmonary Arterial Hypertension Esophageal Varices Amyotrophic Lateral Sclerosis Type 16 Congenital Venous Malformation Hyperlipidemia Chronic Liver Disease Tyrosinemia Type 1 Porphyria Cutanea Tarda Autosomal Recessive Mental Retardation Type 27 Alcoholic Liver Disease Alcoholic Ketoacidosis Autosomal Recessive Mental Retardation Type 31 Neonatal Inflammatory Skin and Bowel Disease Atypical Hemolytic Uremic Syndrome BAP1-Related Tumor Predisposition Syndrome Alcoholic Fatty Liver Pitt-Hopkins-Like Syndrome Type 2 Chorea PANDAS Mycobacterium Intracellulare Infection Distal Myopathy Type Tateyama May-Thurner Syndrome Congenital Bile Acid Synthesis Defect Type 4 Injury of Collateral Ligament of the Knee Cognitive Impairment - Cerebellar Ataxia Sclerosteosis Type 2 EDICT Syndrome Cerebellar Disease Hypermethioninemia due to Adenosine Kinase Deficiency Substance Withdrawal Syndrome Multiple Mitochondrial Dysfunctions Syndrome Type 2 Toxic Myocarditis Mitochondrial Membrane Protein-Associated Neurodegeneration Hereditary ATTR Amyloidosis Venous Disorder of Lower Extremity Myoglobinuria Hydatidiform Mole 2