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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