15601 to 15700 most common queries

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

• Lethal Congenital Contracture Syndrome 6
• Long QT Syndrome 14
• Combined Oxidative Phosphorylation Deficiency Type 24
• Charcot-Marie-Tooth Disease Type 2T
• Progressive Myoclonic Epilepsy Type 8
• Osteogenesis Imperfecta Type 16
• Congenital Myasthenic Syndrome 14
• Focal Segmental Glomerulosclerosis Type 9
• Congenital Fibrosis of Extraocular Muscles Type 5
• Autosomal Dominant Thrombocytopenia 5
• Lissencephaly 6 with Microcephaly
• Early Infantile Epileptic Encephalopathy Type 28
• Autosomal Recessive Spinocerebellar Ataxia 18
• Ruijs Aalfs Syndrome
• Polyglucosan Body Myopathy Type 2
• Autosomal Recessive Mental Retardation Type 47
• Retinal Dystrophy and Obesity
• Progressive Myoclonic Epilepsy Type 7
• Platelet-Type Bleeding Disorder 19
• Autosomal Recessive Microcephaly with Chorioretinopathy Type 2
• Macular Dystrophy with Central Cone Involvement
• Familial Thoracic Aortic Aneurysm 9
• Nemaline Myopathy Type 10
• Charcot-Marie-Tooth Disease Type 2S
• Hypomyelinating Leukodystrophy Type 9
• Early Infantile Epileptic Encephalopathy Type 27
• Autosomal Recessive Spinocerebellar Ataxia Type 17
• Immunodeficiency Type 38 with Basal Ganglia Calcification
• Macular Degeneration, Early Onset
• Autosomal Recessive Mental Retardation Type 46
• Familial Cold Autoinflammatory Syndrome Type 4
• Polyendocrine - Polyneuropathy Syndrome
• Mitochondrial Complex 3 Deficiency Nuclear Type 9
• Autoimmune Lymphoproliferative Syndrome Type 5
• Immunodeficiency Type 37
• Muscular Dystrophy-Dystroglycanopathy Type C12
• SIFD Syndrome
• Autosomal Dominant Mental Retardation Type 30
• Pontocerebellar Hypoplasia Type 1C
• Autosomal Recessive Primary Microcephaly Type 12
• Proliferating Angioendotheliomatosis
• Autosomal Dominant Mental Retardation Type 29
• Neonatal Inflammatory Skin and Bowel Disease 2
• Small Intestinal Angiodysplasia
• Early Infantile Epileptic Encephalopathy Type 26
• Variant Angina Pectoris
• Muscular Dystrophy-Dystroglycanopathy Type C7
• Autosomal Recessive Primary Microcephaly Type 13
• Reflex Sympathetic Dystrophy
• Combined Oxidative Phosphorylation Deficiency 22
• Autosomal Recessive Deafness 103
• Recessive Intermediate Charcot-Marie-Tooth Disease Type D
• Neu-Laxova Syndrome Type 2
• Focal Segmental Glomerulosclerosis Type 8
• Hypogonadotropic Hypogonadism Type 22
• Thoracic Outlet Syndrome
• Adams-Oliver Syndrome Type 5
• Hyperphosphatasia with Mental Retardation Type 5
• Nutcracker Esophagus
• Angelica Extract
• Vertebral Artery Aneurysm
• Mitral Valve Insufficiency
• Focal Segmental Glomerulosclerosis Type 7
• Cerebral Embolism
• Splenic Infarction
• Autosomal Recessive Mental Retardation Type 45
• Cone Rod Dystrophy Type 20
• Cardiac Dyskinesia
• Ventricular Aneurysm
• Vesicoureteral Reflux 8
• Autosomal Recessive Centronuclear Myopathy 5
• Cushing Syndrome due to Macronodular Adrenal Hyperplasia
• Infantile-Onset Multisystem Autoimmune Disease Type 1
• Thoracic Aortic Aneurysm
• Splenic Artery Aneurysm
• Myopia Type 24
• Renal Artery Aneurysm
• Autosomal Recessive Mental Retardation Type 44
• Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3
• Popliteal Artery Aneurysm
• Popliteal Aneurysm
• Peripheral Arteriovenous Aneurysm
• Progressive Encephalopathy with Lipodystrophy
• Lower Extremity Arterial Aneurysm
• Epiphyseal Chondrodysplasia Type Miura
• Retinitis Pigmentosa 70
• Jugular Foramen Syndrome
• Internal Carotid Artery Aneurysm
• Tapia's Syndrome
• Hereditary Hemorrhagic Telangiectasia
• Dilated Cardiomyopathy 1NN
• Hepatic Artery Aneurysm
• Frontotemporal Dementia with Motor Neuron Disease Type 2
• Ductus Arteriosus Aneurysm
• Diamond-Blackfan Anemia Type 13
• Lymphatic Malformation Type 4
• Early Infantile Epileptic Encephalopathy Type 25
• Spinal and Bulbar Muscular Atrophy
• Papilledema
• Platelet-Type Bleeding Disorder 18