14601 to 14700 most common queries

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

• Ruijs Aalfs Syndrome
• Progressive Myoclonic Epilepsy Type 7
• Severe Autosomal Recessive Macrothrombocytopenia
• Macular Dystrophy with Central Cone Involvement
• Early Infantile Epileptic Encephalopathy Type 27
• Autosomal Recessive Spinocerebellar Ataxia Type 17
• Macular Degeneration, Early Onset
• Autosomal Recessive Mental Retardation 46
• Proliferating Angioendotheliomatosis
• Neonatal Inflammatory Skin and Bowel Disease 2
• Early Infantile Epileptic Encephalopathy Type 26
• Variant Angina Pectoris
• Autosomal Recessive Limb-Girdle Muscular Dystrophy Type 2U
• Autosomal Recessive Primary Microcephaly 13
• Reflex Sympathetic Dystrophy
• Combined Oxidative Phosphorylation Deficiency 22
• Autosomal Recessive Deafness 103
• Neu-Laxova Syndrome Type 2
• Focal Segmental Glomerulosclerosis Type 8
• Hypogonadotropic Hypogonadism Type 22
• Adams-Oliver Syndrome 5
• Hyperphosphatasia-Intellectual Disability Syndrome 1
• Angelica Extract
• Focal Segmental Glomerulosclerosis Type 7
• Vesicoureteral Reflux 8
• Autosomal Recessive Centronuclear Myopathy 5
• Cushing Syndrome due to Macronodular Adrenal Hyperplasia
• Autosomal Dominant Myopia Type 24
• Renal Artery Aneurysm
• Megalencephaly-Polymicrogyria-Polydactyly-Hydrocephalus Syndrome 3
• Popliteal Artery Aneurysm
• Peripheral Arteriovenous Aneurysm
• Tall Stature-Scoliosis-Macrodactyly of the Great Toes Syndrome
• Dilated Cardiomyopathy 1NN
• Diamond-Blackfan Anemia Type 13
• Hereditary Lymphedema Type 1D
• Early Infantile Epileptic Encephalopathy Type 25
• Bleeding Disorder due to CalDAG-GEFI Deficiency
• Amelogenesis Imperfecta Hypomaturation Type IIA5
• Primary Ciliary Dyskinesia 29
• Early Infantile Epileptic Encephalopathy Type 24
• Early Infantile Epileptic Encephalopathy Type 23
• Early Infantile Epileptic Encephalopathy Type 21
• Left Ventricular Aneurysm
• Anaesthetic Induction Agent
• PGM3-Related Congenital Disorder of Glycosylation
• Abdominal Obesity - Metabolic Syndrome Type 3
• Anesthetic
• General Anesthesia
• Anemone Pulsatilla
• Common Variable Immunodeficiency 11
• Autosomal Dominant Giant Axonal Neuropathy Type 2 
• Ataxia-Telangiectasia-Like Disorder Type 1
• Carbohydrate Deficient Glycoprotein Syndrome Type 1Y
• Autosomal Recessive Ocular Coloboma
• Congenital Hemolytic Anemia
• Bardet-Biedl Syndrome Typ 5
• Generalized Peeling Skin Syndrome
• X-Linked Mental Retardation 100
• Open-Angle Glaucoma 1P
• Autosomal Dominant Myopia 17
• Anemia of Infection
• Autosomal Recessive Spastic Paraplegia Type 45
• Autosomal Dominant Spastic Paraplegia Type 41
• Cataract 21, multiple Types
• Congenital Non-Bullous Ichthyosiform Erythroderma ARCI2
• Y-Linked Deafness 1
• Neonatal Hyperbilirubinemia
• Autosomal Dominant Deafness 33
• Anemarrhena
• Autosomal Recessive Hypohidrotic Ectodermal Dysplasia Type 10B
• Androgen Therapy
• Cortical Dysplasia Complex with Other Brain Malformations 5
• Moyamoya Disease with Early-Onset Achalasia
• Poor Response to Eculizumab
• Early Infantile Epileptic Encephalopathy Type 19
• Nemaline Myopathy 9
• Premature Ovarian Failure Type 9
• Premature Ovarian Failure Type 8
• Pancytopenia - Developmental Delay Syndrome
• Auriculocondylar Syndrome 3
• Analgesic Abuse
• Analbuminemia
• Perianal Warts
• Joubert Syndrome 22 with Orofaciodigital Defect 6
• Squamous Cell Carcinoma of the Anus
• Anakinra
• COASY Protein-Associated Neurodegeneration
• Anagrelide
• Macrocephaly-Developmental Delay Syndrome
• Drug-induced Thrombocytopenia
• Congenital Dyserythropoietic Anemia Type 1
• Autosomal Dominant Deafness 56
• Autosomal Recessive Spastic Paraplegia Type 72
• Fanconi Renotubular Syndrome 3
• L-Ferritin Deficiency
• Congenital Disorder of Glycosylation Type 9
• Nephrotic Syndrome Type 9
• Autoimmune Lymphoproliferative Syndrome Type 3
• Familial Episodic Pain Syndrome