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Lettris is a curious tetris-clone game where all the bricks have the same square shape but different content. Each square carries a letter. To make squares disappear and save space for other squares you have to assemble English words (left, right, up, down) from the falling squares.
Boggle gives you 3 minutes to find as many words (3 letters or more) as you can in a grid of 16 letters. You can also try the grid of 16 letters. Letters must be adjacent and longer words score better. See if you can get into the grid Hall of Fame !
Change the target language to find translations.
Tips: browse the semantic fields (see From ideas to words) in two languages to learn more.
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Analgesia, Congenital, Pain Insensitivity, Congenital - CADASIL, CADASILM - Kallmann's Syndrome, Kallmann Syndrome, Kallmann Syndrome 1, Kallmann Syndrome 2 - Autosomal Chromosome Disorders, Chromosomal Disorders, Chromosome Abnormality Disorders, Chromosome Disorders - Hemoglobinopathies - Cherubism - Progeria, Adult, Werner's Syndrome, Werner Syndrome - Anemia, Hemolytic, Congenital, Congenital Hemolytic Anemia - Blood Coagulation Disorders, Inherited, Coagulation Disorders, Inherited, Hereditary Blood Coagulation Disorders, Hereditary Coagulation Disorders, Inherited Blood Coagulation Disorders, Inherited Coagulation Disorders - Asymmetric Septal Hypertrophy, Familial, Cardiomyopathy, Hypertrophic, Familial - Angioedema, Hereditary, Hereditary Angioedema, Hereditary Angioneurotic Edema - Genetic Diseases, X-Chromosome Linked, Genetic Diseases, X-Linked, X-Linked Genetic Diseases - Hajdu-Cheney Syndrome, Osteolysis, Multicentric - Camurati-Engelmann Disease, Camurati-Engelmann Syndrome, Diaphyseal Dysplasia, Progressive, Engelmann's Disease, Engelmann Disease - Eye Diseases, Hereditary, Hereditary Eye Diseases - Marfan's Syndrome, Marfan Syndrome - Familial Mediterranean Fever, Hereditary Periodic Fever Syndromes, Mediterranean Fever, Familial, Periodic Disease, Periodic Disease, Wolff's, Periodic Fever Syndromes, Hereditary, Wolff's Periodic Disease, Wolff Periodic Disease - Genetic Skin Diseases, Skin Diseases, Genetic - Alagille Syndrome, Alagille Syndrome 1, Alagille Syndrome 2, Alagille-Watson Syndrome, Arteriohepatic Dysplasia, Cholestasis with Peripheral Pulmonary Stenosis, Dysplasia, Arteriohepatic, Hepatic Ductular Hypoplasia, Syndromatic - Fong Disease, Nail-Patella Syndrome, Osteo-Onychodysplasia, Hereditary, Osterreicher Syndrome, Pelvic Horn Syndrome, Turner-Kieser Syndrome - Fragilitas Ossium, Lobstein's Disease, Lobstein Disease, Osteogenesis Imperfecta - Familial Dysalbuminemic Hyperthyroxinemia, Hyperthyroxinemia, Familial Dysalbuminemic - Adrenal Hyperplasia, Congenital, Congenital Adrenal Hyperplasia - Brugada ECG Pattern, Brugada Syndrome, Brugada Type ECG Pattern, Sudden Unexplained Nocturnal Death Syndrome (SUNDS) - Muscular Dystrophies, Muscular Dystrophy - Degenerative Disease, Nervous System, Hereditary, Heredodegenerative Disorders, Nervous System - Ataxia Telangiectasia, Ataxia-Telangiectasia, Ataxia Telangiectasia Syndrome, Louis-Bar Syndrome - Genetic Diseases, Y-Chromosome Linked, Genetic Diseases, Y-Linked, Y-Linked Genetic Diseases - Ciliary Dyskinesia, Primary, Kartagener's Syndrome, Kartagener's Triad, Kartagener Syndrome, Kartagener Triad, Siewert Syndrome - Anemia, Hypoplastic, Congenital, Congenital Hypoplastic Anemia, Hypoplastic Anemia, Congenital - Dwarfism, Nanism - Metabolism, Inborn Errors, Metabolism Errors, Inborn - Cancer Syndromes, Hereditary, Hereditary Cancer Syndromes, Hereditary Neoplastic Syndromes, Neoplastic Syndromes, Hereditary - Cystic Fibrosis, Fibrocystic Disease of Pancreas, Mucoviscidosis, Pancreatic Cystic Fibrosis, Pulmonary Cystic Fibrosis - Congenital Myasthenia Gravis, Congenital Myasthenic Syndromes, Congenital Myasthenic Syndromes, Postsynaptic, Congenital Myasthenic Syndromes, Presynaptic, Congenital Slow-Channel Myasthenic Syndromes, Myasthenia Gravis, Congenital, Myasthenic Syndromes, Congenital, Myasthenic Syndromes, Congenital, Slow Channel, Postsynaptic Congenital Myasthenic Syndromes, Presynaptic Congenital Myasthenic Syndromes, Slow-Channel Congenital Myasthenic Syndromes[Spéc.]
Genetics, Medical, Medical Genetics[Analogie]