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Emery-Dreifuss Muscular Dystrophy Type 2 Rigid Spine Syndrome Congenital Muscular Dystrophy Type Ullrich Muscular Dystrophy-Dystroglycanopathy Type A4 Limb-Girdle Muscular Dystrophy Type 2C Reticulate Acropigmentation of Kitamura Dyschromatosis symmetrica hereditaria Kohlschütter-Tönz Syndrome Witkop Syndrome CHANDS Syndrome Trichodental Syndrome Salamon Syndrome Wiedemann-Rautenstrauch Syndrome Infantile Restrictive Dermopathy Kindler Syndrome Hereditary Benign Telangiectasia X-Linked Nephrolithiasis Type 1 Nephrotic Syndrome Type 1 Amelogenesis Imperfecta Type 1B Complement Factor H Deficiency Recurrent Neisseria Infections due to Factor D Deficiency Congenital Disorder of Glycosylation Type 2C Leukocyte Adhesion Deficiency Type 1 Hyper IgD Syndrome X-Linked Hyper-IgM Syndrome Thromboxane Synthase Deficiency Myeloperoxidase Deficiency Lipedema Congenital Hypomyelinating Neuropathy X-Linked Charcot-Marie-Tooth Disease Type 1 Hereditary Motor and Sensory Neuropathy Type 6 Idiopathic Basal Ganglia Calcification Benign Hereditary Chorea Chorea Acanthocytosis Syndrome Autosomal Recessive Spastic Paraplegia Type 20 Spinal Muscular Atrophy Type 2 Roberts Syndrome Tietz Syndrome Congenital Disorder of Glycosylation Type 1A Birt-Hogg-Dubé Syndrome Gorlin-Chaudhry-Moss Syndrome Familial Cold Autoinflammatory Syndrome Type 1 Deficiency of Interleukin-36-Receptor Antagonist Fish-Eye Disease Dihydropyrimidinuria Thiopurine S-Methyltransferase Deficiency Pearson Syndrome Cytosolic Acetoacetyl-CoA Thiolase Deficiency 3-Methylglutaconic Aciduria Type 1 Transcobalamin 1 Deficiency Dopamine Beta-Hydroxylase Deficiency Woodhouse Sakati Syndrome Thyroglobulin Synthesis Defect Iodotyrosine Deiodinase Deficiency Iodotyrosyl Coupling Defect Eosinophilic Esophagitis Familial Candidiasis Type 4 High Altitude Pulmonary Hypertension Blue Cone Monochromacy Autosomal Dominant Optic Atrophy Frontotemporal Dementia Aplasia Cutis Congenita Hunermann Conradi Syndrome Congenital Antithrombin III Deficiency Cognitive Impairment Positive COVID-19 Test Contact COVID-19 Case Stay in COVID-19 Risk Area Isolated Growth Hormone Deficiency Familial Thyroid Dyshormonogenesis Leukocyte Disorder PLA2G6-Associated Neurodegeneration Neutrophil Chemotactic Response Abnormal Burn Scar Motility-Related Diarrhea Lower Extremity-Predominant Spinal Muscular Atrophy Collagenopathy Type 2 - Collagenopathy Type 11 KCNQ2-Related Disorders Critical Limb Ischemia Precocious Epileptic Encephalopathy Congenital Contracture Localized Hypertrophic Neuropathy Fatal Infantile Encephalomyopathy Anti-HLA Hyperimmunization Benign Reproductive Organ Neoplasm TBC1D24-Related Disorders RRM2B-Related Mitochondrial Disease Myosinopathy Diffuse Hyperinsulinism Vasculitis Syndromes of the Nervous System Cone-Rod Dystrophy - Hearing Loss Sigmoid Disease Laryngeal Cleft Acquired Angioedema with C1Inh Deficiency FBLN5-Related Cutis Laxa Vaginal Endometrial Stromal Neoplasm Bartholin's Gland Disease INSR-Related Severe Syndromic Insulin Resistance Senile Plaque Formation Central Nervous System Hematopoietic Neoplasm