Sitemap | Symptoma 18101 to 18200 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Metabolic Acidosis PEHO Syndrome Hypomyelinating Leukodystrophy Type 3 Pelviscapular Dysplasia Acetone Poisoning Euhidrotic Ectodermal Dysplasia Laryngeal Edema Achromatopsia Type 3 Adult Polyglucosan Body Disease Erectile Dysfunction Periorbital Edema Peroxisomal ACYL-COA Oxidase Deficiency Acrootoocular Syndrome Drug-induced Neutropenia Hypophosphatemia Hunger Pygmy (Disorder) Acidosis Aplastic Anemia Hypokalemia Knobloch Syndrome Type 1 Methemoglobinemia Autosomal-Recessive Robinow Syndrome Acetanilide Poisoning Autosomal Recessive Benign Familial Neonatal Epilepsy Insulin-Like Growth Factor 1 Resistance Hepatic Encephalopathy Autosomal Recessive Spastic Ataxia Type Charlevoix-Saguenay Autosomal Recessive Spastic Paraplegia Type 15 Autosomal Recessive Spastic Paraplegia Type 5A Autosomal Recessive Spinocerebellar Ataxia 3 Heart Failure Hyperglycemia Spastic Ataxia - Corneal Dystrophy Erythema Multiforme Casamassima-Morton-Nance Syndrome Brachyolmia Type Hobaek Brachyolmia Type Toledo Acute Liver Failure Spondylometaepiphyseal Dysplasia - Short Limb - Abnormal Calcification Acetaminophen Overdose Cold-Induced Sweating Syndrome Type 1 Dissecting Aneurysm Spondylocarpotarsal Synostosis Aneurysm Chronic Active Hepatitis Taurodontia Absent Teeth Sparse Hair Massive Hepatic Necrosis Drug-induced Hypoglycemia Familial Thyroid Dyshormonogenesis Type 1 Renal Papillary Necrosis Usher Syndrome Type 2A Usher Syndrome Type 1C Interstitial Nephritis Nonallergic Interstitial Nephritis Methylmalonic Acidemia with Homocystinuria Type cblF Methylmalonic Acidemia with Homocystinuria Type cblC Homocystinuria with Methylmalonic Aciduria Type cblD Asthma Pontocerebellar Hypoplasia Type 2A Waardenburg Syndrome Type 4A Accessory Nerve Palsy CHIME Syndrome Accessory Lobe of Lung Dent Disease Type 1 Pulmonary Disorder Periventricular Nodular Heterotopia Type 1 Gingivostomatitis X-Linked Deafness 4 Gingivitis Early Infantile Epileptic Encephalopathy Type 9 Androgens Aphthous Stomatitis X-Linked Spondyloepimetaphyseal Dysplasia 2p21 Deletion Syndrome Acatalasia Ehlers-Danlos Syndrome Classic-Like Type 1 Huntington Disease-Like 2 Persistent Polyclonal B-cell Lymphocytosis Dominant Intermediate Charcot-Marie-Tooth Disease Type B Ameloblastoma Dominant Intermediate Charcot-Marie-Tooth Disease Type A Homozygous 11p15-p14 Deletion Syndrome Corneal Ulcer Charcot-Marie-Tooth Disease Type 2F Waardenburg Syndrome Type 1 Corneal Opacity Loss of Vision Muscular Dystrophy-Dystroglycanopathy Type B5 Alcohol Consumption Protozoan Infection Spinocerebellar Ataxia Type 15 Skin Infection Thrombosis Acute Hemorrhagic Leukoencephalitis Acanthamoeba Keratitis Kufor-Rakeb Syndrome Agammaglobulinemia Drug Eruptions Gastritis Medicamentosa
