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15601 to 15700 most common queries
List represents a sample of symptoms, diseases, and other queries. Updated weekly.
Long QT Syndrome 15
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