15901 to 16000 most common queries

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

• Age-Related Macular Degeneration 13
• Familial Thoracic Aortic Aneurysm 8
• Hodgkin Lymphoma
• Retinitis Pigmentosa with Situs Inversus
• 3q13.31 Microdeletion Syndrome
• Factor II Deficiency
• Specific Language Impairment 5
• Myopia Type 22
• Edema
• Nephrogenic Diabetes Insipidus
• Autosomal Recessive Primary Microcephaly Type 11
• Nephrotic Syndrome
• Complex Cortical Dysplasia with other Brain Malformations Type 4
• Acute Glomerulonephritis
• Complex Cortical Dysplasia with other Brain Malformations Type 3
• Renal Vein Thrombosis
• Renal Amyloidosis
• Primary Amyloidosis
• Autonomic Neuropathy
• Familial Amyloid Polyneuropathy
• Multiple Congenital Anomalies - Hypotonia - Seizures Type 3
• Meckel Syndrome Type 11
• Hepatosplenic Amyloidosis
• Cutaneous Amyloidosis
• Nephronophthisis 16
• Recessive Intermediate Charcot-Marie-Tooth Disease Type C
• Cone Rod Dystrophy Type 18
• Secondary Amyloidosis
• Myeloma-associated Amyloidosis
• Childhood-Onset Epileptic Encephalopathy
• Amyloidosis in Familial Mediterranean Fever
• Fetal Akinesia - Cerebral and Retinal Hemorrhage Syndrome
• Restrictive Cardiomyopathy
• Estrogen Resistance Syndrome
• Bifascicular Block
• Left Anterior Fascicular Block
• Limb-Girdle Muscular Dystrophy Type 2S
• Muscular Dystrophy-Dystroglycanopathy Type B14
• Muscular Dystrophy-Dystroglycanopathy Type A14
• Left Ventricular Hypertrophy
• Ehlers-Danlos Syndrome Spondylodysplastic Type 2
• Infiltrative Cardiomyopathy
• Central Precocious Puberty Type 2
• Cardiac Amyloidosis
• Idiopathic Familial Pulmonary Arterial Hypertension
• Early Infantile Epileptic Encephalopathy Type 16
• Acute Hemolytic Anemia
• Multiple Mitochondrial Dysfunctions Syndrome Type 3
• Amprenavir
• Shaheen Syndrome
• Toxic Hemolytic Anemia
• Dowling-Degos Disease Type 1
• Ampicillin-Sulbactam
• Perrault Syndrome Type 4
• Adams-Oliver Syndrome Type 4
• Hypersensitivity Myocarditis
• Distal Renal Tubular Acidosis
• Infantile Myofibromatosis Type 2
• Muscular Dystrophy-Dystroglycanopathy Type A13
• Unstable Angina
• Congenital Neutropenia - Myelofibrosis - Nephromegaly Syndrome
• Complex Cortical Dysplasia with other Brain Malformations Type 2
• Bruxism
• Congenital Disorder of Deglycosylation
• Fanconi Anemia Complementation Group Q
• Hypomania
• Hypogonadotropic Hypogonadism Type 21
• Hypogonadotropic Hypogonadism Type 20
• Hypogonadotropic Hypogonadism Type 19 
• Cerebral Angiitis
• Hypogonadotropic Hypogonadism Type 18
• Subarachnoid Hemorrhage
• Hypogonadotropic Hypogonadism Type 17
• Malignant Hypertension
• Muscular Dystrophy-Dystroglycanopathy Type A12
• Nephrotic Syndrome Type 8
• Hypochromic Microcytic Anemia with Iron Overload Type 2
• Drug-induced Cardiomyopathy
• ATP5A1-Related ATP Synthase Deficiency
• Postaxial Polydactyly Type A6
• Xerostomia
• Osteogenesis Imperfecta Type 15
• Oculocutaneous Albinism Type 7
• Hypertensive Encephalopathy
• Heat Stroke
• Familial Episodic Pain Syndrome Type 1
• Autosomal Recessive Monocyte and Dendritic Cell Deficiency
• Autosomal Dominant Aplasia and Myelodysplasia
• Perrault Syndrome 3
• Delusion
• Complex Cortical Dysplasia with other Brain Malformations Type 1
• Acute Amphetamine Intoxication
• Foveal Hypoplasia Type 2
• Amphetamine Withdrawal
• Epileptic Encephalopathy Type Lennox-Gastaut
• Amphetamine
• Amphetamine Delusional Disorder
• Amyotrophic Lateral Sclerosis Type 21
• Autosomal Dominant Cerebellar Ataxia - Deafness - Narcolepsy
• Stevens-Johnson Syndrome