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Posterior Cerebral Artery Thrombosis Cutaneous Mastocytosis - Short Stature - Conductive Hearing Loss - Microtia Immune Hemolytic Anemia Fatal Infantile Lactic Acidosis with Methylmalonic Aciduria Hyperlipidemia due to Hepatic Triglyceride Lipase Deficiency Dactylolysis Spontanea HIV-Associated Enteropathy Catecholaminergic Polymorphic Ventricular Tachycardia Type 3 Cryptococcal Meningitis Lissencephaly 4 with Microcephaly AIDS Dementia Complex Nestor-Guillermo Progeria Syndrome Agrimonia Eupatoria Autosomal Dominant Dyskeratosis Congenita 2 Congenital Neutropenia Combined Pituitary Hormone Deficiency 6 Non-24 Hour Sleep-Wake Disorder Retinitis pigmentosa 60 Diphtheria Hyperphenylalaninemia Anal Fissure Narcolepsy-Cataplexy Syndrome Parasagittal Meningioma Agranulocytosis Non-epileptic Convulsion Agony Parasomnia Type Sleepwalking Pregnancy-related Diabetic Ulcer Agitated Depression Complication of Procedure Attention Deficit Disorder Mass Lesion of the Brain Partial Blindness Partial Acquired Lipodystrophy Associated with C3 Nephritic Factor Middle Cerebral Artery Occlusion Vitreous Floaters Tissue Nematode Infection Dissecting Aortic Aneurysm Poisoning Arteriosclerosis Organophosphate Poisoning Vitamin Deficiency Familial Hypertrophic Cardiomyopathy Type 20 Carcinoma of Bladder Gastric Cancer Familial Hypertrophic Cardiomyopathy Type 18 Colon Carcinoma Aging Familial Hypertrophic Cardiomyopathy Type 17 CNS Metastasis Fatal Infantile Hypertonic Myofibrillar Myopathy Presbyesophagus Retinitis pigmentosa 38 Retinitis Pigmentosa 59 Orofacial Cleft Type 13 Central Retinal Vein Occlusion Bacterial Pneumonia Carcinoma of the Lung Retinopathy Biological Effects of Substances of Abuse Glaucoma Personality Disorder Carcinoma of the Breast Leber Congenital Amaurosis Type 15 Toxic Effect Colonic Angiodysplasia Hereditary Protein C Deficiency Vaginal Adhesions Familial Hypertrophic Cardiomyopathy Type 16 Intracranial Hematoma Lumbar Compression Fracture Multisystemic Smooth Muscle Dysfunction Syndrome Penile Hematoma Systolic Hypertension Progressive Myoclonic Epilepsy Type 5 Senile Angioma Congenital Stationary Night Blindness Type 1D Aortic Valve Calcification Old Age Muscular Dystrophy-Dystroglycanopathy Type C9 Malignant Glioma Ectropion Marital Conflict Acute Leukemia Pontocerebellar Hypoplasia Type 2D Leukemia Intestinal Lymphoma X-Linked Agammaglobulinemia Retinitis pigmentosa 40 Bronchiectasis Aneurysm-Osteoarthritis Syndrome Tobacco Use Complement Component 8 Deficiency Type 1 Amebic Abscess Congenital Agammaglobulinemia Immunodeficiency due to a Late Complement Component Deficiency Chlamydia Trachomatis Infection Pneumococcal Pneumonia Iron Intake