14901 to 15000 most common queries

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

• Psychomotor Retardation - Epilepsy and Craniofacial Dysmorphism
• Lethal Neonatal Spasticity - Epileptic Encephalopathy
• Chronic Anxiety
• Septic Arthritis
• Congenital Cataract-Hearing Loss-Severe Developmental Delay Syndrome
• Transient Infantile Hypertriglyceridemia and Hepatosteatosis
• Atrial Septal Defect 9
• Joubert Syndrome Type 15
• Bleeding Peptic Ulcer
• Esophageal Varices on Barium Swallow
• Autosomal Recessive Cutis Laxa Type 1B
• Water Soluble Vitamin Deficiency
• Congenital Cerulean Cataract Type 5
• Pharyngeal Carcinoma
• Familial Mesial Temporal Lobe Epilepsy with Febrile Seizures
• Familial Temporal Lobe Epilepsy 5
• Nephronophthisis 13
• Autosomal Recessive Mental Retardation 27
• Autosomal Recessive Mental Retardation 31
• Neonatal Inflammatory Skin and Bowel Disease
• BAP1-Related Tumor Predisposition Syndrome
• Alcoholic Fatty Liver
• Pitt-Hopkins-Like Syndrome
• PANDAS
• Mycobacterium Intracellulare Infection
• Distal Myopathy Type Tateyama
• Congenital Bile Acid Synthesis Defect Type 4
• Injury of Collateral Ligament of the Knee
• EDICT Syndrome
• Multiple Mitochondrial Dysfunctions Syndrome Type 2
• Hydatidiform Mole 2
• Autosomal Recessive Stickler Syndrome
• Arthrogryposis, Perthes Disease and Upward Gaze Palsy
• Familial Juvenile Hyperuricemic Nephropathy 3
• Familial Retinal Arterial Macroaneurysm
• Acromioclavicular Separation
• Nocturnal Leg Cramp
• Hereditary Sensory and Autonomic Neuropathy Type 2C
• Hyperphosphatasia with Mental Retardation Syndrome 3
• Hereditary Late-Onset Parkinson Disease Type 17
• Glycoprotein 1A Deficiency
• Nephrotic Syndrome Type 6
• Leber Congenital Amaurosis 16
• Geleophysic Dysplasia 2
• Monocytopenia with Susceptibility to Infections
• Brittle Cornea Syndrome 2
• Autosomal Dominant Myopia 21
• Immunodeficiency Type 31C
• Autosomal Dominant Deafness 64
• Focal Segmental Glomerulosclerosis Type 6
• Hereditary Sensory and Autonomic Neuropathy Type 1E
• Hydrophobia
• Mild Cognitive Impairment
• Multiple Congenital Anomalies - Hypotonia - Seizures Type 1
• Fecal Incontinence
• Chondrodysplasia with Joint Dislocations Type gPAPP
• Hermansky-Pudlak Syndrome Type 7
• Autosomal Recessive Spastic Paraplegia 52
• TMEM70-Related Mitochondrial Encephalo-Cardio-Myopathy
• Familial Atrial Fibrillation Type 12
• Late-onset Depression
• Hypotonia-Failure to Thrive-Microcephaly Syndrome
• Alpha 2 Macroglobulin Deficiency
• Eclipse Blindness
• Glyoxalase II Deficiency
• Posterior Cerebral Artery Occlusion with Infarction
• Progressive Myoclonic Epilepsy Type 6
• Hypotrichosis 8
• Basilar Artery Thrombosis with Occlusion of a Precerebral Artery
• Renal Carcinoma
• Alcoholic Gastritis
• Adamantinoma
• Differentiated Thyroid Gland Carcinoma
• Hypoinsulinemic Hypoglycemia and Body Hemihypertrophy
• Hereditary Thrombophilia due to Congenital Protein S Deficiency
• Ectopic Parathormone Syndrome
• Partial Intestinal Obstruction
• Multiple Mitochondrial Dysfunctions Syndrome Type 1
• ATPAF2-Related ATP Synthase Deficiency
• Acrodysostosis Type 1
• Generalized Arterial Calcification of Infancy 2
• Atrial Septal Defect - Atrioventricular Conduction Defects Syndrome
• Thrombocythemia 2
• Tumor Necrosis Factor Receptor 1-associated Periodic Syndrome
• IFAP Syndrome with or without BRESHEK Syndrome
• Disorder of Basilar Artery
• Pelvic Appendix
• Multiple Congenital Anomalies - Hypotonia - Seizures Type 2
• Amnesia
• X-linked Intellectual Disability Type Kroes
• X-Linked Dominant Chondrodysplasia Type Chassaing-Lacombe
• X-Linked Syndromic Mental Retardation Type Chudley-Schwartz
• Intellectual Disability - Alacrima - Achalasia Syndrome
• Human Albumin
• X-Linked Mental Retardation 96
• Primary Pulmonary Arterial Hypertension
• Autosomal Dominant Osteopetrosis Type 2
• Albinism
• Alagille Syndrome
• Dilated Cardiomyopathy Type 1U