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Lettris
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
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 !
English dictionary
Main references
Most English definitions are provided by WordNet .
English thesaurus is mainly derived from The Integral Dictionary (TID).
English Encyclopedia is licensed by Wikipedia (GNU).
Translation
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analogical dictionary
Cherry Red Spot Myoclonus Syndrome, Deficiency Disease, Ganglioside Sialidase, Ganglioside Sialidase Deficiency Disease, I-Cell Disease, Inclusion Cell Disease, Lipomucopolysaccharidosis, Mucolipidoses, Mucolipidosis, Mucolipidosis I, Mucolipidosis II, Mucolipidosis III, Mucolipidosis IV, Mucolipidosis Type I, Mucolipidosis Type II, Mucolipidosis Type III, Mucolipidosis Type IV, Myoclonus Cherry Red Spot Syndrome, Pseudo-Hurler Polydystrophy, Psuedo-Hurler Disease, Sialidosis, Type III Mucolipidosis, Type II Mucolipidosis, Type I Mucolipidosis, Type IV Mucolipidosis - Carboxylase Deficiency, Combined, Carboxylase Deficiency, Multiple, Combined Carboxylase Deficiency, Deficiency, Combined Carboxylase, Deficiency, Multiple Carboxylase, Multiple Carboxylase Deficiency - Mucopolysaccharidoses, Mucopolysaccharidosis - Carbohydrate-Deficient Glycoprotein Syndrome, Glycoprotein Syndrome, Carbohydrate-Deficient - alpha-Fucosidase Deficiency Disease, alpha-L-Fucosidase Deficiency Disease, Deficiency Disease, alpha-Fucosidase, Deficiency Disease, alpha-L-Fucosidase, Fucosidase Deficiency Disease, Fucosidosis, Fucosidosis, Infantile, Fucosidosis, Juvenile, Fucosidosis Type I, Fucosidosis Type II - Fructose Metabolism, Inborn Errors - Mannosidase Deficiency Diseases, Mannosidase Deficiency Syndromes, Mannosidosis - Deficiency, Glucosephosphate Dehydrogenase, Glucosephosphate Dehydrogenase Deficiency - Lactose Intolerance, Lactose Malabsorption - Deficiency Disease, Galactokinase, Deficiency Disease, Galactose-1-Phosphate Uridyl-Transferase, Deficiency Disease, UDP-Galactose-4-Epimerase, Deficiency Disease, UDPglucose 4-Epimerase, Galactokinase Deficiency Disease, Galactose-1-Phosphate Uridyl-Transferase Deficiency Disease, Galactosemia, Classic, Galactosemias, UDP-Galactose-4-Epimerase Deficiency Disease, UDPglucose 4-Epimerase Deficiency Disease, UDPglucose-Hexose-1-Phosphate Uridylyltransferase Deficiency, UTP Hexose-1-Phosphate Uridylyltransferase Deficiency - Glycogenosis, Glycogen Storage Disease - Pyruvate Metabolism, Inborn Errors - Hyperoxaluria, Primary, Oxaluria, Primary[Spéc.]
C16.320.565.202 • C18.452.648.202 • Carbohydrate Metabolism, Inborn Error (n.) • Carbohydrate Metabolism, Inborn Errors (n.)