Sitemap | Symptoma 18601 to 18700 most common queries List represents a sample of symptoms, diseases, and other queries. Updated weekly. Paralytic Ileus Goldberg-Shprintzen Syndrome Thromboembolism Amyotrophic Lateral Sclerosis Type 17 Myopathy Myofibrillar Type 5 Subphrenic Abscess Autosomal Recessive Deafness 23 Gastric Fistula Resistance to Clopidogrel Colonic Pseudo-Obstruction Spastic Paraplegia - Optic Atrophy - Neuropathy Peritoneal Abscess Abdominal Wall Hematoma Aicardi-Goutières Syndrome Type 4 Pneumoperitoneum Familial Anomalous Origin of Right Pulmonary Artery Deep Vein Thrombosis Autosomal Dominant Nocturnal Frontal Lobe Epilepsy Type 4 Pulmonary Embolism Retinal Cone Dystrophy Type 3B Portal Vein Thrombosis Autosomal Recessive Spastic Paraplegia Type 30 Abdominal Surgery Enteric Anendocrinosis Myopathy Autosomal Recessive Ichthyosis with Hypotrichosis ARCI11 Congenital Malrotation of the Colon Congenital Disorder of Glycosylation Type 1M Epiphyseal Dysplasia Type Baumann Nonsyndromic Renal Hypodysplasia Type 1 Prune Belly Syndrome Holoprosencephaly Type 9 Myxomatous Mitral Valve Prolapse 3 Vomiting Stroke Cluster Headache Leri Pleonosteosis Platyspondylic Lethal Skeletal Dysplasia Type Torrance Migraine Equivalent Li-Fraumeni Syndrome 1 Microcephaly - Chorioretinopathy - Lymphedema - Mental Retardation School Phobia Phobia Malingering Mesomelic Dysplasia Type Kantaputra Conversion Disorder Irritable Bowel Syndrome Holoprosencephaly Type 2 Autosomal Dominant Progressive External Ophthalmoplegia Type 1 Motion Sickness Abdominal Migraine Familial Mixoploidy Distal Hereditary Motor Neuropathy Type 7A Distal Hereditary Motor Neuropathy Type 2A Bethlem Myopathy Abdominal Mass Myoclonus-Dystonia Syndrome 11 Small Bowel Obstruction Jankovic Rivera Syndrome Thoracic Duct Obstruction Autosomal Dominant Centronuclear Myopathy Peritoneal Adhesion Cardiomyopathy Dilated 1S Abdominal Radiation Leigh Syndrome of Adult Congenital Myopathy with Excess of Thin Filaments Retinitis Pigmentosa 27 Abdominal Epilepsy Neuronal Ceroid Lipofuscinosis Type 4B Congenital Neuropathy with Arthrogryposis Multiplex Abdominal Aortic Thrombosis Abdominal Aortic Aneurysm Repair Congenital Nystagmus 2, Autosomal Dominant Vascular Disease Blepharofacioskeletal Syndrome Ischemic Bowel Disease Oculo-Pharyngo-Distal Myopathy Weight Loss Hereditary Distal Onycholysis Autosomal Dominant Optic Atrophy - Hearing Loss - Peripheral Neuropathy Syndrome Acute Superior Mesenteric Artery Insufficiency Autosomal Dominant Optic Atrophy and Cataract Gnathodiaphyseal Dysplasia Constipation Inclusion Body Myopathy - Paget Disease - Frontotemporal Dementia Paroxysmal Extreme Pain Disorder Spondyloepiphyseal Dysplasia Type Reardon Familial Hypertryptophanemia Lethal Neonatal Carnitine Palmitoyl Transferase II Deficiency Severe Infantile Carnitine Palmitoyl Transferase II Deficiency Late-Onset Carnitine Palmitoyl Transferase II Deficiency Komuragaeri Disease Autosomal Recessive Inclusion Body Myopathy Type 2 Distal Hereditary Motor Neuropathy Type 5A Behavioral Variant of Frontotemporal Dementia Abdominal Angina Familial Hypertrophic Cardiomyopathy Type 6 Charcot-Marie-Tooth Disease Type 2B Intestinal Disease Surgical Wound Infection
