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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).
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analogical dictionary
Acquired Metabolic Diseases, Brain, Acquired Metabolic Diseases, Nervous System, Acquired Metabolic Encephalopathies, Brain Diseases, Metabolic, Brain Diseases, Metabolic, Acquired, Brain Disorders, Metabolic, Brain Disorders, Metabolic, Acquired, Brain Syndrome, Metabolic, Brain Syndrome, Metabolic, Acquired, Central Nervous System Metabolic Disorders, CNS Metabolic Disorders, CNS Metabolic Disorders, Acquired, Encephalopathies, Metabolic, Encephalopathy, Metabolic, Acquired, Metabolic Brain Diseases, Metabolic Brain Diseases, Acquired, Metabolic Brain Syndrome, Metabolic Brain Syndrome, Acquired, Metabolic Brain Syndromes, Metabolic Brain Syndromes, Acquired, Metabolic Diseases, Acquired, Nervous System, Metabolic Disorder, Central Nervous System, Acquired, Metabolic Disorders, Brain, Metabolic Disorders, Central Nervous System, Metabolic Disorders, CNS, Metabolic Disorders, CNS, Acquired, Metabolic Encephalopathies, Nervous System Acquired Metabolic Diseases - Metabolism, Inborn Errors, Metabolism Errors, Inborn[Hyper.]
Cerebral Pseudosclerosis, Hepatic Form of Wilson Disease, Hepatocerebral Degeneration, Hepatolenticular Degeneration, Hepato-Neurologic Wilson Disease, Kinnier-Wilson Disease, Neurohepatic Degeneration, Progressive Lenticular Degeneration, Pseudosclerosis, Westphal-Strumpell Syndrome, Wilson's Disease, Wilson Disease, Wilson Disease, Hepatic Form - Amino Acid Transport Disorder, Neutral, Hartnup Disease - Choreoathetosis Self-Mutilation Hyperuricemia Syndrome, Complete HGPRT Deficiency Disease, Deficiency Disease, Complete HGPRT, Deficiency Disease, Hypoxanthine-Phosphoribosyl-Transferase, HGPRT Deficiency Disease, Complete, Hypoxanthine-Phosphoribosyl-Transferase Deficiency Disease, Lesch-Nyhan Disease, Lesch-Nyhan Syndrome - Cerebral Amyloid Angiopathy, Familial, Cerebral Amyloid Angiopathy, Genetic, Cerebral Amyloid Angiopathy, Hereditary, Dutch Type Hereditary Cerebral Amyloid Angiopathy, Familial Cerebral Amyloid Angiopathy, Hereditary Cerebral Amyloid Angiopathy, Hereditary Cerebral Amyloid Angiopathy, Dutch Type, Hereditary Cerebral Amyloid Angiopathy, Icelandic Type, Icelandic Type Amyloidosis, Icelandic Type Hereditary Cerebral Amyloid Angiopathy - Cystathionine beta-Synthase Deficiency Disease, Deficiency Disease, Cystathionine beta-Synthase, Homocystinuria - Deficiency Disease, Dihydropteridine Reductase, Deficiency Disease, Phenylalanine Hydroxylase, Deficiency Disease, Phenylalanine Hydroxylase, Severe, Dihydropteridine Reductase Deficiency Disease, Folling's Disease, Fölling's disease, Folling Disease, Hyperphenylalaninaemia, Hyperphenylalaninemia, Non-Phenylketonuric, Phenylalanine Hydroxylase Deficiency Disease, Phenylalanine Hydroxylase Deficiency Disease, Severe, Phenylketonuria, Phenylketonuria, Atypical, Phenylketonuria, Classical, Phenylketonuria I, Phenylketonuria II, Phenylketonurias - Branched-Chain Ketoaciduria, Classical Maple Syrup Urine Disease, Classic Maple Syrup Urine Disease, Intermediate Maple Syrup Urine Disease, Intermittent Maple Syrup Urine Disease, Maple Syrup Urine Disease, Maple Syrup Urine Disease, Classic, Maple Syrup Urine Disease, Classical, Maple Syrup Urine Disease, Intermediate, Maple Syrup Urine Disease, Intermittent, Maple Syrup Urine Disease, Thiamine Responsive, MSUD (Maple Syrup Urine Disease), Thiamine Responsive Maple Syrup Urine Disease - 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 - Congenital Hypocupremia, Hypocupremia, Congenital, Kinky Hair Disease, Kinky Hair Syndrome, Menkes' Disease, Menkes Disease, Menkes Kinky Hair Syndrome, Menkes Syndrome, Steely Hair Disease, Steely Hair Syndrome - MELAS Syndrome, Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode - Deficiency Disease, Ornithine Carbamoyltransferase, Deficiency Disease, Ornithine Transcarbamylase, ornithine, Ornithine Carbamoyltransferase Deficiency Disease, Ornithine Transcarbamylase Deficiency Disease - Arginase Deficiency Disease, Argininemia, Deficiency Disease, Arginase, Hyperargininemia - 4-Hydroxyphenol Pyruvic Acid Oxidase Deficiency Disease, 4 Hydroxyphenylpyruvate Dioxygenase Deficiency Disease, Deficiency Disease, 4-Hydroxyphenol Pyruvic Acid Oxidase, Deficiency Disease, Fumarylacetoacetase, Deficiency Disease, Tyrosine Transaminase, Fumarylacetoacetase Deficiency Disease, Hereditary Tyrosinemia, Type I, Hereditary Tyrosinemia, Type II, Hereditary Tyrosinemia, Type III, Hypertyrosinemia, Type I, Tyrosinemia, Type I, Tyrosinemia, Type II, Tyrosinemia, Type III, Tyrosinemias, Tyrosinemias, Hereditary, Tyrosine Transaminase Deficiency Disease - Lysosomal Enzyme Disorders, Nervous System, Lysosomal Storage Diseases, Nervous System, Nervous System Lysosomal Enzyme Disorders, Nervous System Lysosomal Storage Diseases - Adrenoleukodystrophy, Neonatal, Hyperpipecolic Acidemia, Peroxisomal Disorders, Peroxisomal Dysfunction, General, Peroxisomal Dysfunction, Multiple, Peroxisomal Dysfunction, Single - Ataxia with Lactic Acidosis, Type I, Juvenile Pyruvate Dehydrogenase Complex Deficiency Disease, Lactic Acidosis with Ataxia, Type I, Neonatal Pyruvate Dehydrogenase Complex Deficiency Disease, PDHC Deficiency Disease, Pyruvate Dehydrogenase Complex Deficiency Disease, Pyruvate Dehydrogenase Complex Deficiency Disease, Juvenile, Pyruvate Dehydrogenase Complex Deficiency Disease, Neonatal, Type I Ataxia with Lactic Acidosis - Hyperglycinemia, Nonketotic, Hyperglycinemia, Nonketotic, Type I, Hyperglycinemia, Nonketotic, Type II, Hyperglycinemia, Nonketotic, Type III, Nonketotic Hyperglycinemia, Nonketotic Hyperglycinemia, Type I, Nonketotic Hyperglycinemia, Type II, Nonketotic Hyperglycinemia, Type III, Type III Nonketotic Hyperglycinemia, Type II Nonketotic Hyperglycinemia, Type I Nonketotic Hyperglycinemia - Argininosuccinate Synthase Deficiency Disease, Argininosuccinic Acid Synthase Deficiency Disease, Argininosuccinic Acid Synthetase Deficiency, Complete, Argininosuccinic Acid Synthetase Deficiency Disease, Argininosuccinic Acid Synthetase Deficiency Disease, Partial, Citrullinemia, Citrullinemia, Classical, Citrullinemia, Late-Onset, Citrullinemia, Neonatal, Citrullinuria, Complete Argininosuccinic Acid Synthetase Deficiency Disease, Deficiency, Argininosuccinic Acid Synthetase, Complete, Deficiency, Argininosuccinic Acid Synthetase, Partial, Deficiency Disease, Argininosuccinate Synthase, Deficiency Disease, Argininosuccinic Acid Synthase, Partial Argininosuccinic Acid Synthetase Deficiency Disease - Cerebrooculorenal Syndrome, Cerebro-Oculo-Renal Syndrome, Lowe-Bickel Syndrome, Lowe Disease, Lowe Oculocerebrorenal Syndrome, Lowe Syndrome, Lowe-Terrey-MacLachlan Syndrome, Oculocerebrorenal Dystrophy, Oculocerebrorenal Syndrome, Renal-Oculocerebrodystrophy - Carbamoyl Phosphate Synthase (Ammonia) Deficiency Disease, Carbamoyl-Phosphate Synthase I Deficiency Disease - Encephalomyelitis, Subacute Necrotizing, Encephalomyelopathy, Subacute Necrotizing, Encephalopathy, Subacute Necrotizing, Encephalopathy, Subacute Necrotizing, Infantile, Encephalopathy, Subacute Necrotizing, Juvenile, Infantile Leigh Disease, Infantile Subacute Necrotizing Encephalopathy, Juvenile Leigh Disease, Juvenile Subacute Necrotizing Encephalopathy, Leigh's Disease, Leigh Disease, Leigh Disease, Infantile, Leigh Disease, Juvenile, Leigh Syndrome, Subacute Necrotizing Encephalomyelitis, Infantile, Subacute Necrotizing Encephalopathy, Subacute Necrotizing Encephalopathy, Infantile, Subacute Necrotizing Encephalopathy, Juvenile - Fukuhara Disease, Fukuhara Syndrome, MERRF Syndrome, Myoclonic Epilepsy and Ragged Red Fibers, Myoclonic Epilepsy with Ragged Red Fibers - Alpha-Aminoadipic Semialdehyde Deficiency Disease, Deficiency Disease, Alpha-Aminoadipic Semialdehyde, Deficiency Disease, Lysine Alpha-Ketoglutarate Reductase, Deficiency Disease, Saccharopine Dehydrogenase, Hyperlysinemia, Familial, Hyperlysinemia, Periodic, Hyperlysinemias, Lysine Alpha-Ketoglutarate Reductase Deficiency Disease, Saccharopine Dehydrogenase Deficiency Disease - Ataxia with Lactic Acidosis, Type II, Deficiency Disease, Pyruvate Carboxylase, Lactic Acidosis with Ataxia, Type II, Pyruvate Carboxylase Deficiency Disease, Type II Ataxia with Lactic Acidosis[Spéc.]
Brain Diseases, Metabolic, Familial (n.) • Brain Diseases, Metabolic, Inborn (n.) • Brain Diseases, Metabolic, Inherited (n.) • Brain Syndrome, Metabolic, Inborn (n.) • C10.228.140.163.100 • C16.320.565.189 • C18.452.132.100 • C18.452.648.189 • Central Nervous System Inborn Metabolic Diseases (n.) • Central Nervous System Inborn Metabolic Disorders (n.) • CNS Metabolic Disorders, Inborn (n.) • Encephalopathies, Metabolic, Inborn (n.) • Familial Metabolic Brain Diseases (n.) • Familial Metabolic Disorders, Brain (n.) • Inborn Errors of Metabolism, Brain (n.) • Inborn Metabolic Brain Diseases (n.) • Inborn Metabolic Brain Disorders (n.) • Inborn Metabolic Disorders, Brain (n.) • Inherited Metabolic Brain Diseases (n.) • Inherited Metabolic Disorders, Brain (n.) • Metabolic Brain Diseases, Familial (n.) • Metabolic Brain Diseases, Inborn (n.) • Metabolic Brain Diseases, Inherited (n.) • Metabolic Brain Syndrome, Inborn (n.) • Metabolic Diseases, Inborn, Brain (n.) • Metabolic Diseases, Inborn, Central Nervous System (n.) • Metabolic Disorders, Brain, Inherited (n.) • Metabolic Disorders, CNS, Inborn (n.) • Metabolic Disorders, Familial, Brain (n.)