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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
Anomalie congénitale, Anomalie morphologique congénitale, Anomalies congénitales, Anomalies morphologiques congénitales, Difformités congénitales, Malformation, Malformations — Abnormalities, Congenital, Birth Defects, Congenital Abnormalities, Congenital Defects, Defects, Congenital, Deformities - Anomalies monogéniques, génopathie, Génopathies, Génopathies monogéniques, Maladie héréditaire, Maladies génétiques congénitales, Maladies héréditaires, Maladies monogéniques — Genetic Diseases, Inborn, Hereditary Disease, Hereditary Diseases, Inborn Genetic Diseases, Single-Gene Defects[Hyper.]
Délétion 5p, Délétion 5p-, Délétion du bras court du chromosome 5, Maladie du cri-du-chat, Monosomie 5p, Syndrome du cri du chat, Syndrome du cri-du-chat — 5p Deletion Syndrome, 5p- Syndrome, Chromosome 5p- Syndrome, Chromosome 5 Short Arm Deletion Syndrome, Cri-du-Chat Syndrome, Crying Cat Syndrome, Deletion of Short Arm of Chromosome 5 Syndrome - Syndrome d'Angelman, Syndrome de la marionnette joyeuse, Syndrome du pantin hilare — Angelman Syndrome, Happy Puppet Syndrome, Puppet Children - Arhinencéphalie, Holoprosencéphalie, Holoprosencéphalie alobaire, Holoprosencéphalie lobaire, Holoprosencéphalie semilobaire, Holoprosencéphalie semi-lobaire — Alobar Holoprosencephaly, Arhinencephaly, Holoprosencephaly, Lobar Holoprosencephaly, Semilobar Holoprosencephaly - Mongolisme, Syndrome de Down, Syndrome de Down avec trisomie partielle, Trisomie 21, Trisomie 21 par non-disjonction méiotique, Trisomie 21 par non-disjonction mitotique — Down's Syndrome, Down Syndrome, Down Syndrome, Partial Trisomy 21, Mongolism, Partial Trisomy 21 Down Syndrome, Trisomy 21, Trisomy 21, Meiotic Nondisjunction, Trisomy 21, Mitotic Nondisjunction - Syndrome de Brachmann-De Lange, Syndrome de Cornelia De Lange, Syndrome de De Lange, Typus amstelodamensis — Brachmann-De Lange Syndrome, Cornelia De Lange Syndrome, De Lange's Syndrome, De Lange Syndrome, Typus Degenerativus Amstelodamensis - Délétion distale 4p, Délétion télomérique 4p, Délétion terminale 4p, Monosomie distale 4p, Syndrome de Pitt-Rogers-Danks, Syndrome de Wolf-Hirchhorn — Pitt-Rogers-Danks Syndrome, Wolf-Hirchhorn Syndrome, Wolf-Hirschhorn Syndrome - Syndrome BOR, Syndrome branchio-oculo-facial, Syndrome branchio-oto-rénal — BOR Syndrome, Branchio-Oculo-Facial Syndrome, Branchio-Otorenal Dysplasia, Branchio-Otorenal Syndrome, Branchio-Oto-Renal Syndrome - Omphalocèle-macroglossie-gigantisme, SBW (Syndrome de Beckwith-Wiedemann), Syndrome de Beckwith-Wiedemann, Syndrome de Wiedemann-Beckwith, Syndrome omphalocèle-macroglossie-gigantisme — Beckwith-Wiedemann Syndrome, Exomphalos-Macroglossia-Gigantism Syndrome, Wiedemann-Beckwith Syndrome - Syndrome de la face d'elfe, Syndrome de Williams, Syndrome de Williams-Beuren, Syndrome de Williams et Beuren — Contiguous Gene Syndrome, Williams, Elfin Facies Syndrome, Williams-Beuren Syndrome, Williams Contiguous Gene Syndrome, Williams Syndrome - Syndrome de Prader-Labhart-Willi, Syndrome de Prader-Willi, Syndrome de Prader-Willi (SPW), Syndrome de Royer — Labhart-Willi-Prader-Fanconi Syndrome, Labhart-Willi Syndrome, Prader-Willi Syndrome, Royer's Syndrome, Royer Syndrome - Maladies chromosomiques gonosomiques, Maladies liées aux chromosomes sexuels, Troubles liés aux chromosomes sexuels — Disorders, Sex Chromosome, Disorders, Sex Chromosome Abnormality, Sex Chromosome Abnormality Disorders, Sex Chromosome Disorders - Syndrome associant tumeur de Wilms-aniridie-malformations génito-urinaires-retard mental, Syndrome WAGR, WAGR Complex, WAGR Contiguous Gene Syndrome, Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome — Contiguous Gene Syndrome, WAGR, WAGR Syndrome - SRT (Syndrome de Rubinstein-Taybi), Syndrome de Rubinstein et Taybi, Syndrome de Rubinstein-Taybi, Syndrome des pouces et des gros orteils trop larges — Broad Thumb-Hallux Syndrome, Rubinstein Syndrome, Rubinstein-Taybi Syndrome - Délétion 11q23, Délétion 11q terminale, Délétion distale 11q, PTS (Paris-Trousseau Syndrome), Syndrome de Jacobsen, Syndrome de Paris-Trousseau, Syndrome Paris-Trousseau, Thrombocytopénie de Paris-Trousseau, Thrombocytopénie type Paris-Trousseau, Trouble de délétion terminale du chromosome 11q — 11q23 Deletion Disorder, 11q Deletion Disorder, 11q Deletion Syndrome, 11q Terminal Deletion Disorder, Jacobsen Distal 11q Deletion Syndrome, Jacobsen Syndrome, Jacobsen Thrombocytopenia, Paris-Trousseau Syndrome, Paris-Trousseau Thrombocytopenia[Spéc.]
Autosomal Chromosome Disorders (n.) • C16.131.260 • C16.320.180 • Chromosomal Disorders (n.) • Chromosome Abnormality Disorders (n.) • Chromosome Disorders (n.) • Maladies autosomiques (n.) • Maladies chromosomiques (n.) • Maladies chromosomiques autosomiques (n.)