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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
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 - down (syndrome de), 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 - Naevomatose basocellulaire, Naevomatose baso-cellulaire, NBC (Naevomatose BasoCellulaire), Syndrome de carcinome basocellulaire naevoïde, Syndrome de Gorlin, Syndrome de Gorlin-Goltz, Syndrome du carcinome naevoïde basocellulaire — Basal Cell Nevus Syndrome, Gorlin Syndrome, Nevoid Basal Cell Carcinoma Syndrome, Nevus Syndrome, Basal Cell - Syndrome de Prune Belly, Syndrome de Prune-Belly — Prune Belly Syndrome, Prune-Belly Syndrome - Dysostoses oro-digito-faciales, Syndrome de Mohr, Syndrome de Papillon-Léage et Psaume, Syndrome de Papillon-Léage-Psaume, Syndrome orodigitofacial, Syndrome oro-digito-facial, Syndrome oro-facio-digital, Syndrome oro-facio-digital de type 1, Syndrome oro-facio-digital de type 2, Syndrome oro-facio-digital de type I, Syndrome oro-facio-digital de type II, Syndromes oro-facio-digitaux — Gorlin-Psaume Syndrome, Mohr Syndrome, Orofaciodigital Syndromes, Papillon-Leage and Psaume Syndrome - Aplasie cutanée congénitale, Aplasie ectodermique congénitale, Dysplasie ectodermique, Dysplasie ectodermique anhidrotique, Dysplasie ectodermique hidrotique, Syndrome de Clouston — Anhidrotic Ectodermal Dysplasia, Anhydrotic Ectodermal Dysplasia, Aplasia Cutis Congenita, Clouston's Syndrome, Congenital Ectodermal Defect, Defect, Congenital Ectodermal, Ectodermal Defect, Congenital, Ectodermal Dysplasia, Hidrotic Ectodermal Dysplasia, Hydrotic Ectodermal Dysplasia - SBB (Syndrome de Bardet-Biedl), Syndrome de Bardet-Biedl — Bardet-Biedl Syndrome, Laurence-Moon-Bardet-Biedl Syndrome - Arhinencéphalie, Holoprosencéphalie, Holoprosencéphalie alobaire, Holoprosencéphalie lobaire, Holoprosencéphalie semilobaire, Holoprosencéphalie semi-lobaire — Alobar Holoprosencephaly, Arhinencephaly, Holoprosencephaly, Lobar Holoprosencephaly, Semilobar Holoprosencephaly - Maladie de Zellweger, Syndrome cérébro-hépato-rénal, Syndrome de Zellweger, Syndrome de Zellweger-like — Cerebrohepatorenal Syndrome, Cerebro-Hepato-Renal Syndrome, Zellweger's Syndrome, Zellweger Disease, Zellweger-Like Syndrome, Zellweger Syndrome - Syndrome d'Angelman, Syndrome de la marionnette joyeuse, Syndrome du pantin hilare — Angelman Syndrome, Happy Puppet Syndrome, Puppet Children - Syndrome de Bloom, Syndrome de Bloom-Torre-Machacek — Bloom Syndrome, Bloom-Torre-Machacek Syndrome - 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 - Dysplasie artériohépatique, Dysplasie artério-hépatique, Paucité des voies biliaires syndromique, Paucité ductulaire syndromatique, Syndrome d'Alagille, Syndrome d'Alagille 1, Syndrome d'Alagille-1, Syndrome d'Alagille 2, Syndrome d'Alagille-2 — Alagille Syndrome, Alagille Syndrome 1, Alagille Syndrome 2, Alagille-Watson Syndrome, Arteriohepatic Dysplasia, Cholestasis with Peripheral Pulmonary Stenosis, Dysplasia, Arteriohepatic, Hepatic Ductular Hypoplasia, Syndromatic - prader-labhart-willi (syndrome de), 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 - Syndrome de Gardner — Gardner Syndrome - Syndrome de Beemer, Syndrome de Majewski, Syndrome de Saldino-Noonan, Syndrome des côtes courtes-polydactylie, Syndrome des côtes courtes-polydactylie de 4, Syndrome des côtes courtes-polydactylie de III, Syndrome des côtes courtes-polydactylie de IV, Syndrome des côtes courtes-polydactylie de type 1, Syndrome des côtes courtes-polydactylie de type 2, Syndrome des côtes courtes-polydactylie de type 3, Syndrome des côtes courtes-polydactylie de type I, Syndrome des côtes courtes-polydactylie de type II, Syndrome des côtes courtes-polydactylie type Beemer, Syndrome des côtes courtes-polydactylie type Majewski, Syndrome des côtes courtes-polydactylie type Saldino-Noonan, Syndrome des côtes courtes-polydactylie type Verma-Naumoff, Syndrome de Verma-Naumoff — Majewski Syndrome, Saldino-Noonan Syndrome, Short Rib-Polydactyly Syndrome - Embryofoetopathie rubéolique, Embryo-foetopathie rubéolique, Rubéole congénitale, Rubéole congénitale malformative, SRC (Syndrome de Rubéole Congénitale), Syndrome de rubéole congénitale — Congenital Rubella Syndrome, Rubella Syndrome, Congenital, Syndrome, Congenital Rubella - 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 - Naevus sébacé de Jadassohn, Naevus sébacé linéaire, Syndrome de Feuerstein-Mims-Schimmelpenning, Syndrome de Jadassohn-Schimmelpenning-Feuerstein-Mims, Syndrome de l'hamartome sébacé, Syndrome de naevus sébacé linéaire, Syndrome de Schimmelpenning-Feuestein-Mims — Feuerstein-Mims Syndrome, Jadassohn Nevus Phakomatosis, Linear Sebaceous Nevus Syndrome, Nevus, Linear Sebaceous, Nevus Sebaceous of Jadassohn, Organoid Nevus Phakomatosis, Schimmelpenning-Feuerstein-Mims Syndrome, Schimmelpenning Syndrome, Sebaceous Nevus of Jadassohn - Lentiginose cardiomyopathique, léopard (syndrome), Syndrome des lentigines multiples, Syndrome LEOPARD — LEOPARD Syndrome, Multiple Lentigines Syndrome - Nanisme progéroïde, Syndrome de Cockayne, Syndrome de Cockayne groupe A, Syndrome de Cockayne groupe B, Syndrome de Cockayne groupe C, Syndrome de Cockayne type 1, Syndrome de Cockayne type 2, Syndrome de Cockayne type 3, Syndrome de Cockayne type A, Syndrome de Cockayne type B, Syndrome de Cockayne type C, Syndrome de Cockayne type I, Syndrome de Cockayne type II, Syndrome de Cockayne type III — Cockayne Syndrome, Cockayne Syndrome, Group A, Cockayne Syndrome, Group B, Cockayne Syndrome, Group C, Cockayne Syndrome, Type A, Cockayne Syndrome, Type B, Cockayne Syndrome, Type C, Cockayne Syndrome, Type I, Cockayne Syndrome, Type II, Cockayne Syndrome, Type III, Group A Cockayne Syndrome, Group B Cockayne Syndrome, Group C Cockayne Syndrome, Progeria-Like Syndrome, Type A Cockayne Syndrome, Type B Cockayne Syndrome, Type C Cockayne Syndrome, Type I Cockayne Syndrome, Type II Cockayne Syndrome, Type III Cockayne Syndrome - Syndrome de Lowe, Syndrome oculocérébrorénal, Syndrome oculo-cérébro-rénal, Syndrome oculo-cérébro-rénal de Lowe — 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 - DIDMOAD, Syndrome de Wolfram — DIDMOAD, Wolfram 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 - Gigantisme partiel-hémihypertrophie-macrocéphalie, Proteus-Like Syndrome, Syndrome de Protée — Elephant Man Disease, Proteus Syndrome - Dolichosténomélie, Maladie de Marfan, Syndrome de Marfan — Marfan's Syndrome, Marfan Syndrome - Diplégie faciale congénitale, Paralysie oculofaciale congénitale de Moebius, Syndrome de Mobius, Syndrome de Moebius — Congenital Oculofacial Paralysis, Moebius, Mobius Syndrome, Moebius Congenital Oculofacial Paralysis, Moebius Syndrome - laurence-moon-bardet-biedl (syndrome de), Syndrome de Laurence-Moon, Syndrome de Laurence-Moon-Biedl — Laurence-Moon-Biedl Syndrome, Laurence-Moon Syndrome - Syndrome de Klein, Syndrome de Klein-Waardenburg, Syndrome de Waardenburg, Syndrome de Waardenburg avec anomalies des membres supérieurs, Syndrome de Waardenburg de type 3, Syndrome de Waardenburg de type III, waardenburg (syndrome de) — Klein's Syndrome, Klein-Waardenburg Syndrome, Waardenburg's Syndrome, Waardenburg-Klein Syndrome - Incontinentia pigmenti, Syndrome de Bloch-Sulzberger — Bloch-Sulzberger Syndrome, Incontinentia Pigmenti - Maladie de Fong, Onycho-arthro-ostéodysplasie héréditaire, Onycho-ostéodysplasie héréditaire, Onycho-ostéo-dysplasie héréditaire, Ostéo-onychodysostose, Ostéo-onychodysplasie héréditaire, Syndrome d'Österreicher, Syndrome de Turner-Kieser, Syndrome nail-patella — Fong Disease, Nail-Patella Syndrome, Osteo-Onychodysplasia, Hereditary, Osterreicher Syndrome, Pelvic Horn Syndrome, Turner-Kieser Syndrome - Surdité-cécité, Surdité-cécité-mutisme, Surdité-mutisme-cécité, Syndromes avec surdité-cécité, Troubles auditifs et visuels, Troubles de l'audition et de la vision — Blind-Deaf Disorders, Blindness-Deafness, Deaf-Blind Disorders, Deaf-Blindness Disorders, Deaf-Blind Syndromes, Deaf-Mutism-Blind Disorders, Deafness-Blindness, Hearing and Vision Loss, Prelingual Deaf-Blind Disorders, Prelingual Deafness-Blindness, Vision and Hearing Loss - 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 Amish-cheveux épars, Syndrome BIDS, Syndrome PIBIDS, Trichothiodystrophie avec photosensibilité, Trichothiodystrophie non photosensible de type 1, Trichothiodystrophies, TTD (TrichoThioDystrophie), TTD de type D, TTD de type F — BIDS Syndrome, Photosensitive Trichothiodystrophy, PIBIDS Syndrome, Trichothiodystrophy, Nonphotosensitive 1, Trichothiodystrophy Syndromes - Déficit en 7-déhydrocholestérol réductase, Syndrome de Smith-Lemli-Opitz de type 1, Syndrome de Smith-Lemli-Opitz de type 2, Syndrome de Smith-Lemli-Opitz de type I, Syndrome de Smith-Lemli-Opitz de type II, Syndrome de Smith-Lemli-Optiz, Syndrome RSH-SLO — RSH-SLO Syndrome, RSH Syndrome, Smith-Lemli-Opitz Syndrome, Smith-Lemli-Opitz Syndrome, Type I, Smith-Lemli-Opitz Syndrome, Type II - 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 - poems (syndrome), Syndrome de Crow-Fukase, Syndrome de Takatsuki, Syndrome POEMS — Crow-Fukase Syndrome, POEMS Syndrome, Takatsuki's Syndrome[Spéc.]
Abnormalities, Multiple (n.) • Anomalies congénitales multiples (n.) • Anomalies multiples congénitales (n.) • C16.131.077 • Malformations multiples (n.) • Multiple Abnormalities (n.)