������� ��������� ������� ��� ���������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows\n����� �� ������ ��������� �� ������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� ������ ������ ������������ ������ Microsoft Windows. �������� ������ ������������ ������� Windows ��� �������� �������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460:\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows XP 32-bit\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows XP 64-bit\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows Vista 32-bit\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows Vista 64-bit\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows7 32-bit\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows7 64-bit\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows8 32-bit\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows8 64-bit\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Windows10\n���� ��� ��������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� ��������� ������������ ������� Windows, �� ��� �� ������ ������� �� ������� ����. ��������� �������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ������ ������������� � ������� "��������������".\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Microsoft Windows Server 2003\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Microsoft Windows Server 2008\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Microsoft Windows Server 2008R2\n������� ������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� Microsoft Windows Server 2012\n��������! ���� �� ������ ������ ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� ��� ���������� ���� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460, �� ��� ���������� ���������� ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 � ��������� ������������ �������� ��� ��������-��������. �������� ����� �������� �� ��, ��� ����������� ������ ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ����� ���� ������� � ��� ������, ���� �� �������� ������� ������������ ����������. ��� ����� ���� ������ ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� ������������� ������������ ���������� 1Gb PCI-E DDR-5 MSI MS-V232 N460GTX-MD1GD5-OC (RTL) D-Sub DVI HDMI SLI GeForce GTX460 ��� ���������� ���������.


Zatch Bell #115 - Rodeux's Fierce Attack. Dying Rein. Awaken, Kyle. (TV anime) - Anime Vice\nRodeux's Fierce Attack. Dying Rein. Awaken, Kyle. Rodeux's Fierce Attack. Dying Rein. Awaken, Kyle. is an anime episode of Zatch Bell\nAdd a credit to Rodeux's Fierce Attack. Dying Rein. Awaken, Kyle.. (No voice actors. Add voice actors to characters above.)


HOME » Vena Cava, Inferior (x) » Rymsdyk, Jan van, fl. 1750-1788 (x) » Langerak, Johan Arnold (x) » Anderloni, Faustino, 1766-1847 (x) » Thorax (x) » A series of engravings, accompanied with explanations, which are intended to illustrate <i>The morbid anatomy of some of the most important parts of the human body</i>. Fasciculus 1[-10] ... (x) » Wilson, Erasmus, Sir, 1809-1884 (x) » Innys, William, d. 1756 (x) » Trachea (x) » Pailloux (x) » Search results


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Watchlist\tRandom article\tRecent changes\tChanges: Serpent Ward (Warcraft III)\nRevision as of 04:24, July 16, 2009 (edit)Rolandius (Talk | contribs) (Added Serpent Ward) Latest revision as of 03:56, August 3, 2009 (edit)(undo)Rolandius (Talk | contribs) m (Added image) Line 1:\n[[Image:Serpentward.gif|right|thumb|The Serpent Ward in Warcraft III.]]\n'''Serpent Wards''' are [[serpent]]ine [[ward]]s that are used to attack a [[Shadow Hunter]]'s enemies.\nLatest revision as of 03:56, August 3, 2009


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OCLC:607731405\n1 online resource (xv, 953 pages,  pages of plates) : illustrations (some color)\nBlue diaper syndrome --\nBlue rubber bleb nevus syndrome --\nBook syndrome --\nBoomerang dysplasia --\nBörjeson-forssman-lehmann syndrome --\nBorrone dermato-cardio-skeletal syndrome --\nBoucher-neuhäuser syndrome --\nBouveret syndrome --\nBowen syndrome --\nBowen-conradi syndrome --\nBrachmann-de lange syndrome --\nBrachydactyly-ectrodactyly syndrome with fibular aplasia or hypoplasia --\nBrachymorphism-onychodysplasia-dysphalangism syndrome --\nBranchial myoclonus with spastic paraparesis and cerebellar ataxia syndrome --\nBranchio-oculo-facial syndrome --\nBranchio-skeleto-genital syndrome --\nBrauer syndrome --\nBrittle hair and mental deficit syndrome --\nBronze baby syndrome --\nBrown-vialetto-van laere syndrome --\nBruyn-scheltens syndrome --\nBurton syndrome --\nBuschke-ollendorff syndrome --\nWagr syndrome --\nBrunner winter syndrome --\nC syndrome --\nCacchi-ricci disease --\nCahmr syndrome --\nCalderon gonzalez-cantu syndrome --\nCamfak syndrome --\nCamptodactyly syndrome, guadalajara types i and ii --\nCamurati-engelmann syndrome --\nCanavan syndrome --\nCantalamessa-baldiniambrosi syndrome --\nCantu syndrome --\nCapos syndrome --\nCarbon baby syndrome --\nCardiogenital syndrome --\nCarey-fineman-ziter syndrome --\nCarmi syndrome --\nCarnevale-canun-mendoza syndrome --\nCarnevale-hernandez-castillotorres syndrome --\nCarnevale-krajewska-fischetto syndrome --\nCarney complex --\nCarnitine deficiency --\nCarnitine palmitoyltransferase deficiency --\nCaroli disease and caroli syndrome --\nCartilage-hair hypoplasia syndrome --\nCartwright-nelson-fryns syndrome --\nCastleman disease --\nCastro-gago-pombonovo syndrome --\nCat cry syndrome --\nCataract-alopecia-sclerodactyly syndrome --\nCatlin marks --\nCavernous sinus syndrome --\nCayler syndrome --\nCcge syndrome --\nCecato-de lima-pinheiro syndrome --\nCenani syndactylism --\nCennamo gangemi magli syndrome --\nCephaloskeletal dysplasia --\nCerebral aneurysm-cirrhosis syndrome --\nCerebro-oculo-skeleto-renal syndrome --\nCerebro-reno-digital syndrome --\nCerebrocortical degeneration of infancy --\nCeroid storage disease --\nCeruloplasmin deficiency --\nCervico-oculo-acoustic syndrome --\nCharge syndrome --\nCharlie m syndrome --\nChauffard syndrome --\nChediak-higashi syndrome --\nChemke-oliver-mallek syndrome --\nChild syndrome --\nCholinesterase deficiency --\nChondrodysplasia giant cell type --\nChondrodysplasia grebe type --\nChondrodysplasia-pseudohermaphroditism syndrome --\nChorioretinal dysplasia-microcephaly-mental retardation syndrome --\nChrist-siemens-touraine syndrome --\nChronic granulomatous disease --\nChudley mental retardation syndrome --\nChudley-rozdilsky-houston syndrome --\nCleft hand and absent tibia syndrome --\nCleft-limb-heart malformation syndrome --\nCleft palate lateral synechiae syndrome --\nCleidorhizomelic syndrome --\nCloverleaf skull --\nCoach syndrome --\nCoats disease --\nCodas syndrome --\nCoffin-siris syndrome --\nCohen syndrome --\nCold agglutinin syndrome --\nCold hypersensitivity syndrome --\nCole-carpenter syndrome --\nColeman-randall syndrome --\nCollins-dennis-clarke-pope syndrome --\nComplete androgen insensitivity syndrome --\nComplex disease/deficiency (overview) --\nComplex i deficiency --\nComplex ii deficiency --\nComplex iii deficiency --\nComplex iv deficiency --\nComplex v deficiency --\nCone-rod retinal dystrophies --\nCongenital afibrinogenemia --\nCongenital atresia of larynx --\nCongenital disorders of glycosylation --\nCongenital dyserythropoietic anemias --\nCongenital factor vii deficiency --\nCongenital muscular dystrophy: an overview --\nCongenital myopathy with fiber-type disproportion --\nCongenital pancreatic agenesis --\nCongenital pseudarthrosis of clavicle --\nCongenital pulmonary hypoplasia --\nCongenital shortness of the costocoracoid ligament --\nCongenital stridor --\nConn syndrome --\nCooks syndrome --\nCorneal cerebellar syndrome --\nCorneodermatoosseous syndrome --\nCostello syndrome --\nCousin-walbaum-cegarra syndrome --\nCowchock syndrome --\nCowden syndrome --\nCramer-niederdellmann syndrome --\nCrane-heise syndrome --\nCraniodiaphyseal dysplasia --\nCraniofrontonasal dysplasia --\nCraniomicromelic syndrome --\nCrest syndrome --\nCrigler-najjar syndrome --\nCumming syndrome --\nCuratolo-cilio syndrome --\nCutis laxa --\nCystic hygroma --\nCystinosis. D-2-hydroxyglutaric aciduria --\nDa silva syndrome --\nDanbolt-closs syndrome --\nDarier-white disease --\nDe die smulders vles fryns syndrome --\nDe morsier syndrome --\nDe sanctis cacchione syndrome --\nDe toni debré fanconi syndrome --\nDeafness-optic atrophy syndrome --\nDegos syndrome --\nDejerine-sottas syndrome --\nDelleman oorthuys syndrome --\nDent disease --\nDenys-drash syndrome --\nDermatomyositis and polymyositis --\nDesbuquois syndrome --\nDevriendt legius fryns syndrome --\nD-glyceric acidemia --\nDiencephalic syndrome --\nDiferrante syndrome --\nDigitotalar dysmorphism --\nDihydropyrimidinase deficiency --\nDihydropyrimidine dehydrogenase deficiency --\nDionisi vici sabetta gambarara syndrome --\nDisaccharide intolerance type i --\nDisaccharide intolerance type ii --\nDonnai-barrow syndrome --\nDonohue syndrome --\nDoor syndrome --\nDrachtman weinblatt sitarz syndrome --\nDu pan syndrome --\nDuane retraction syndrome --\nDubin-johnson syndrome --\nDubowitz syndrome --\nDuker weiss siber syndrome --\nDyggve-melchior-clausen syndrome --\nDyke-davidoff-masson syndrome --\nDyskeratosis congenita --\nDysplasia epiphysealis hemimelica --\nEastman-bixler syndrome --\nEbstein syndrome --\nEctodermal dysplasia, ectrodactyly, and macular dystrophy (eem) syndrome --\nEctrodactyly, ectodermal dysplasia, and clefting (eec) syndrome --\nEhlers-danlos syndrome (eds): an overview --\nEhlers-danlos syndrome (eds) --\nEisenmenger reaction --\nElejalde syndrome --\nEmery-dreifuss muscular dystrophy (edmd) --\nEosinophilic endomyocardial disease --\nEpidermal nevus syndrome --\nEpstein syndrome --\nErb and klumpke palsy --\nErdheim-chester disease (ecd) --\nEronen syndrome --\nErythema multiforme (em) --\nEssential thrombocythemia --\nF syndrome --\nFacio-oculo-acoustico-renal (foar) syndrome --\nFacio-thoraco-genital syndrome --\nFamilial amyotrophic dystonic paraplegia --\nFamilial atrial myxoma --\nFamilial benign copper deficiency --\nFamilial generalized anhidrosis --\nFamilial hyperaldosteronism --\nFamilial hypogonadotrophic eunuchoidism --\nFamilial inverted choreoathetosis --\nFamilial juvenile nephronophthisis (nph) --\nFamilial nonchromaffin paragangliomas --\nFamilial osteodysplasia --\nFamilial porencephaly --\nFamilial progressive scleroderma --\nFanconi-bickel syndrome (fbs) --\nFarber uzman syndrome --\nFaulk epstein jones syndrome --\nFeigenbaum bergeron richardson syndrome --\nFeingold syndrome --\nFelty syndrome --\nFemoral-facial syndrome --\nFemur-fibula-ulna syndrome --\nFenton wilkinson toselano syndrome --\nFetal aminopterin syndrome --\nFetal cocaine syndrome --\nFg syndrome --\nFibrin stabilizing factor (factor xiii) deficiency --\nFibrocystic pulmonary dysplasia --\nFloating-harbor syndrome (fhs) --\nFoix alajouanine syndrome --\nForsius-ericksson syndrome --\nFreeman-sheldon syndrome (fss) --\nFriedreich ataxia (frda) --\nFronto-metaphyseal dysplasia of gorlin (fmd) --\nFrydman cohen karmon syndrome --\nGangliosidosis (gm1) type i --\nGangliosidosis (gm2) type ii --\nGarcia-lurie syndrome --\nGeleophysic dysplasia --\nGenoa syndrome --\nGeroderma osteodysplastica syndrome --\nGerstmann-sträussler disease. Gianotti-crosti syndrome --\nGilbert syndrome --\nGilles de la tourette syndrome --\nGitelman syndrome --\nGlucose phosphate isomerase deficiency --\nGlutaric acidemia type i (ga-i) --\nGlutaric acidemia type ii (ga-ii) --\nGlycogen storage diseases (gsd): an overview --\nGlycogen storage disease type 0 --\nGlycogen storage disease type i (gsd i) --\nGlycogen storage disease type ii --\nGlycogen storage disease type iii (gsd iii) --\nGlycogen storage disease type iv (gsd iv) --\nGlycogen storage disease type v (gsd v) --\nGlycogen storage disease type vi (gsd vi) --\nGlycogen storage disease type vii (gsd vii) --\nGlycogen storage disease type viii (gsd viii) --\nGoldston syndrome --\nGoltz syndrome --\nGoodman camptodactyly --\nGoodpasture syndrome --\nGordon-holmes syndrome --\nGordon hyperkalemia-hypertension syndrome --\nGorham-stout disease --\nGorlin-chaudry-moss syndrome --\nGorlin-goltz syndrome --\nGottron syndrome --\nGradenigo syndrome --\nGraham-boyle-troxell syndrome --\nGrand-kaine-fulling syndrome --\nGranddad syndrome --\nGrant syndrome --\nGriscelli syndrome --\nGrisel syndrome --\nGrix-blankenship-peterson syndrome --\nGroenblad-strandberg syndrome --\nGroll-hirschowitz syndrome --\nGsell-erdheim syndrome --\nGuizar-vasquez-luengas syndrome --\nGullner syndrome --\nGunn syndrome --\nHageman factor (factor xii) deficiency --\nHaim munk syndrome --\nHajdu cheney syndrome --\nHakim-adams syndrome --\nHall riggs syndrome --\nHallerman-streiff syndrome --\nHallervorden-spatz disease --\nHaltia-santavuori syndrome --\nHanot-chauffard syndrome --\nHappy puppet syndrome --\nHarboyan syndrome --\nHard syndrome --\nHardcastle syndrome --\nHartnup disease --\nHdr syndrome --\nHecht syndrome --\nHemoglobin disorders: overview --\nHemolytic anemia, congenital, with emphysema and cutis laxa --\nHemophagocytotic lymphohistiocytosis (hlh) --\nHemophilia b --\nHennekam syndrome --\nHereditary acromelalgia --\nHereditary desmoid disease (hdd) --\nHereditary keratitis --\nHereditary motor sensory neuropathies (hmsn): overview --\nHereditary neurocutaneous angiomatoses: overview --\nHereditary neurocutaneous angioma --\nHereditary pancreatitis --\nHereditary sensory and autonomic neuropathies (hsan): overview --\nHereditary stomatocytosis --\nHereditary telangiectasia --\nHereditary vitamin d-resistant rickets (hvdrr) --\nHereditary xerocytosis --\nHermansky-pudlak syndrome (hps) --\nHhh syndrome --\nHhhh syndrome --\nHirschsprung syndrome --\nHomocystinuria (hcu) --\nHorton syndrome --\nHunter syndrome --\nHuntington chorea (hc) --\nHurler syndrome --\nHypereosinophilic syndrome (hes) --\nHyperlipoproteinemia: an overview --\nHyperoxaluria, primary --\nHypoplasia of the right ventricle --\nIce syndrome --\nI-cell disease --\nIchthyosis vulgaris --\nIdiopathic thrombocytopenia purpura --\nImerslund syndrome --\nImmotile cilia syndrome --\nImmunodeficiency centromeric instability and facial anomalies syndrome --\nInclusion body myopathy --\nInfantile pyloric stenosis --\nInfantile sialic acid storage disease --\nInfantile-onset spinocerebellar ataxia (iosca) --\nInfertile male syndrome --\nIntestinal pseudoobstruction caused by neuronal disease --\nIridogoniodysgenesis syndrome --\nIsaacs mertens syndrome --\nIschiopatellar dysplasia --\nIsotretinoin embryopathy-like syndrome --\nIsovaleric acidemia --\nIvic syndrome --\nJacobs syndrome --\nJacobsen syndrome --\nJaffe-lichtenstein syndrome --\nJeune syndrome --\nJob syndrome --\nJohanson-blizzard syndrome (jbs) --\nJohnson munson syndrome --\nJones syndrome --\nJuberg-hayward syndrome --\nJuberg-marsidi syndrome --\nJudge misch wright syndrome --\nJumping frenchman of maine syndrome --\nJung wolff back stahl syndrome --\nJuvenile hyaline fibromatosis --\nJuvenile intestinal polyposis --\nJuvenile myoclonic epilepsy (jme) --\nJuvenile paralysis agitans of hunt. Juvenile sulfatidosis syndrome --\nKaler-garrity-stern syndrome --\nKallmann syndrome --\nKantaputra-gorlin syndrome --\nKaplowitz-bodurtha syndrome --\nKapur-toriello syndrome --\nKarandikar-maria-kamble syndrome --\nKarsch-neugebauer syndrome --\nKartagener syndrome --\nKashani-strom-utley syndrome --\nKasznica-carlson-coppedge syndrome --\nKatsantoni-papadakou-lagoyanni syndrome --\nKatz syndrome --\nKaufman oculo-cerebro-facial syndrome --\nKaveggia syndrome --\nKawashima-tsuji syndrome --\nKbg syndrome --\nKearns-sayre syndrome --\nKennerknecht-vogel syndrome --\nKenny-caffey syndrome --\nKeratitis ichthyosis deafness (kid) syndrome --\nKeratitis, hereditary --\nKeratosis palmaris et plantaris: overview --\nKeratosis palmoplantaris with esophageal cancer --\nKersey syndrome --\nKetoacidosis of infancy --\nKeutel syndrome --\nKhalifa-graham syndrome --\nKikuchi-fujimoto disease --\nKindler syndrome --\nKing-denborough syndrome --\nKinky hair syndrome --\nKinsbourne syndrome --\nKleine-levin hibernation syndrome --\nKleiner-holmes syndrome --\nKlinefelter syndrome xxy/xyy --\nKnobloch syndrome --\nKöbberling-dunnigan syndrome --\nKocher-debré-sémélaigne syndrome --\nKonigsmark syndrome --\nKorula-wilson-salomon syndrome --\nKostmann syndrome --\nKosztolanyi syndrome --\nKousseff-nichols syndrome --\nKousseff syndrome --\nKowarski syndrome --\nKozlowski-brown-hardwick syndrome --\nKozlowski-celermajer syndrome --\nKozlowski-ouvrier syndrome --\nKozlowski-rafinski-kucharska syndrome --\nKozlowski-tsuruta-taki syndrome --\nKozlowski-warren-fisher syndrome --\nKrasnow-qazi syndrome --\nKrause-kivlin syndrome --\nKrause-reese syndrome --\nKrauss-herman-holmes syndrome --\nKrieble-bixler syndrome --\nKudo-tamura-fuse syndrome --\nKumar-levick syndrome --\nKunze-riehm syndrome --\nKurczynski-casperson syndrome --\nKuster-majewski-hammerstein syndrome --\nKuzniecky syndrome --\nKyrle disease. L-2-hydroxyglutaric aciduria --\nLaband syndrome --\nLacrimo-auriculo-dento-digital syndrome (ladd syndrome) --\nLafora syndrome or disease --\nLambert syndrome --\nLandau-kleffner syndrome (lks) --\nLandouzy-dejerine dystrophy --\nLaron syndrome --\nLarsen syndrome --\nLaryngo-onycho-cutaneous (loc) syndrome --\nLaunois syndrome --\nLaurence moon syndrome (lms) --\nLeber congenital amaurosis (lca) --\nLeber hereditary optic neuropathy (lhon) --\nLeigh syndrome --\nLeiner syndrome --\nLemierre syndrome --\nLenz syndrome --\nLenz-majewski syndrome --\nLeopard syndrome --\nLeri pleonosteosis --\nLéri-weill syndrome --\nLetterer-siwe disease (lsd) --\nLeukocyte adhesion deficiency (lad) syndrome --\nLeukodystrophies: overview --\nLeukonychia and other nail discoloration: overview --\nLeukonychia totalis --\nLiddle syndrome --\nLi-fraumeni syndrome (lfs) --\nLightwood syndrome --\nLimb deficiency-heart malformation syndrome --\nLimb-girdle muscular dystrophy (lgmd) --\nLipofuscinoses, neuronal ceroid: overview --\nLoken senior syndrome --\nLong qt syndrome (lqts) --\nLouis-bar syndrome --\nLown-ganong-levine syndrome --\nLowry-wood syndrome --\nLucey-driscoll syndrome --\nLujan fryns syndrome --\nLutembacher syndrome --\nLyell syndrome --\nLymphedema hypoparathyroidism syndrome --\nLymphedema with distichiasis --\nLymphoreticular syndrome --\nLynch syndrome --\nLysinuric protein intolerance --\nMacrocephaly, hypertelorism, short limbs, and hearing loss syndrome --\nMaffucci syndrome --\nMajocchi disease --\nMalpuech syndrome --\nMaple syrup urine disease (msud) --\nMarden-walker syndrome --\nMarinesco-sjögren syndrome --\nMaroteaux cohen-solal bonaventure syndrome --\nMaroteaux-lamy syndrome --\nMarshall syndrome --\nMarshall-smith syndrome --\nMasa syndrome --\nMauriac syndrome --\nMayer-von rokitansky-küster-hauser syndrome --\nMckusick-kaufman syndrome --\nMcpherson-clemens syndrome --\nMeckel-gruber syndrome (mks) --\nMedian cleft facial syndrome --\nMeier-gorlin syndrome --\nMeigs syndrome (including pseudo-meigs syndrome) --\nMelanoma-astrocytoma syndrome --\nMelas syndrome --\nMelnick-fraser syndrome --\nMelnick-needles syndrome (mns) --\nMeltzer syndrome --\nMenkes syndrome --\nMeretoja syndrome --\nMerlob syndrome --\nMerrf syndrome --\nMesomelia-synostoses syndrome --\nMetaphyseal chondrodysplasia, jansen type --\nMetaphyseal chondrodysplasia, mckusick type --\nMetaphyseal chondrodysplasia, schmid type --\nMethemoglobinemia (congenital) --\nMethionine malabsorption syndrome --\nMethylmalonic acidemia (mma) --\nMeyer-betz disease --\nMichels syndrome --\nMicrogastria-limb reduction defects association --\nMicrovillous inclusion syndrome --\nMelanoma-astrocytoma syndrome. Melas syndrome --\nMidas syndrome --\nMiller-dieker lissencephaly syndrome --\nMiller disease --\nMiller fisher syndrome --\nMiller syndrome --\nMilroy disease --\nMilton disease --\nMinicore disease with external ophthalmoplegia --\nMitochondrial acetoacetyl-coa thiolase (acat) deficiency --\nMohr syndrome --\nMohr-tranebjaerg syndrome --\nMollica pavone antener syndrome --\nMoloney syndrome --\nMolybdenum cofactor deficiency --\nMomo syndrome --\nMoore-federman syndrome --\nMoore-smith-weaver syndrome --\nMorgagni-stewart-morel syndrome --\nMorning glory syndrome --\nMorquio syndrome --\nMount reback syndrome --\nMoyamoya syndrome --\nMoynahan alopecia syndrome --\nMuckle-wells syndrome --\nMucopolysaccharidosis (mps) --\nMuir-torre syndrome (mts) --\nMulibrey nanism syndrome --\nMuller barth menger syndrome --\nMulticore myopathy --\nMultiple carboxylase deficiency --\nMultiple epiphyseal dysplasia (med) --\nMultiple synostoses syndrome --\nMyoadenylate deaminase deficiency --\nMyocerebellar disorder --\nMyopathy, distal, welander type --\nMyotubular myopathy --\nMyhre syndrome --\nN syndrome --\nN-acetylglutamate synthetase deficiency --\nNance-horan syndrome --\nNarp syndrome --\nNélaton syndrome --\nNemaline rod myopathy --\nNeonatal lupus erythematosus --\nNeurocutaneous melanosis --\nNeurofibromatosis generalisata --\nNeuronal ceroid lipofuscinoses --\nNezelof syndrome --\nNonketotic hyperglycinemia --\nNyssen-van bogaert syndrome --\nOculocerebral with hypopigmentation syndrome --\nOculodentodigital syndrome --\nOculogastrointestinal muscular dystrophy --\nOdontotrichomelic syndrome --\nOgilvie syndrome --\nOmenn syndrome --\nOndine syndrome --\nOpitz-frias syndrome --\nOral-facial-digital syndrome (ofd) --\nOrnithine carbamoyltransferase deficiency (otcd) --\nOrnithine delta-aminotransferase deficiency --\nOrotic aciduria --\nOtopalatodigital (opd) syndrome type i --\nOtopalatodigital (opd) syndrome type ii --\nOtospondylomegaepiphyseal dysplasia --\nPachydermoperiostosis (pdp) --\nPagod syndrome --\nPallister-hall syndrome --\nPapillon-lefèvre syndrome --\nParana hard skin syndrome --\nParoxysmal cold hemoglobinuria --\nParoxysmal nocturnal hemolytic (pnh) anemia --\nParry-romberg syndrome --\nPatterson pseudo-leprechaunism syndrome --\nPearson syndrome --\nPelizaeus-merzbacher syndrome --\nPena-shokeir syndrome type i --\nPena-shokeir syndrome type ii --\nPendred syndrome --\nPenta x syndrome --\nPep syndrome --\nPeriodic paralysis (pp) --\nPernicious anemia --\nPerrault syndrome --\nPettigrew syndrome --\nPhace syndrome --\nPhosphoenolpyruvate carboxykinase deficiency --\nPhosphoglycerate kinase deficiency --\nPickwickian syndrome --\nPitt-rogers-danks syndrome --\nPitt-williams brachydactyly syndrome --\nPituitary dwarfism --\nPlott syndrome --\nPoland syndrome --\nPoland-moebius syndrome --\nPolip syndrome --\nPollitt syndrome --\nPolyarteritis nodosa (pan) --\nPolycystic kidney disease (pkd) --\nPolycystic liver disease --\nPolyostotic osteolytic dysplasia --\nPorokeratosis of mibelli --\nPotter syndrome --\nPowell venencie gordon syndrome --\nPrader-labhart-willi syndrome --\nPrimary pulmonary hypertension (pph) --\nPrimary torsion dystonia --\nProgeria syndrome --\nProgressive bulbar palsy of childhood --\nProgressive familial intrahepatic cholestasis (pfic) --\nProlidase deficiency --\nPropionic acidemia --\nProximal muscular dystrophy --\nPsaume syndrome --\nPseudo-achondroplastic dysplasia --\nPterygium syndrome --\nPulmonary alveolar microlithiasis --\nPulmonary arteriovenous malformation --\nPurine nucleoside phosphorylase deficiency --\nPurtscher disease --\nPyle disease --\nPyruvate carboxylase deficiency --\nPyruvate dehydrogenase complex deficiency --\nPyruvate kinase deficiency (pkd). Qazi markouizos syndrome --\n(de) quervain thyroiditis --\nQuincke edema --\nRabson-mendenhall syndrome --\nRadial aplasia syndrome --\nRadio-ulnar synostosis --\nRamban-hasharon syndrome --\nRamon syndrome --\nRamsay hunt syndrome type i --\nRamsay hunt syndrome type ii --\nRaynaud syndrome --\nRear syndrome --\nReardon wilson cavanagh syndrome --\nRecombinant chromosome 8 syndrome --\nRefetoff syndrome --\nRefsum syndrome --\nReifenstein syndrome --\nRenal-coloboma syndrome --\nRenal tubular dysgenesis --\nReticular dysgenesia --\nRetino-hepato-endocrinologic syndrome --\nReynolds neri hermann syndrome --\nRhizomelic chondrodysplasia punctata type i --\nRichards rundle syndrome --\nRiley-smith syndrome --\nRitscher-schinzel syndrome --\nRogers syndrome --\nRolland-desbuquois syndrome --\nRombo syndrome --\nRosenberg-chutorian syndrome --\nRosenthal-kloepfer syndrome --\nRosewater syndrome --\nRosseli-gulienetti syndrome --\nRothmann makai syndrome --\nRothmund-thomson syndrome --\nRotor syndrome --\nRoussy-levy syndrome --\nRud syndrome --\nRukavina type amyloid polyneuropathy --\nRundles-falls syndrome --\nRussell weaver bull syndrome --\nRutledge lethal multiple congenital anomaly syndrome --\nRuvalcaba syndrome --\nSabin-feldman syndrome --\nSalt-depletion syndrome --\nSandifer syndrome --\nSandrow syndrome --\nSanjad-sakati syndrome --\nSc phocomelia syndrome --\nSchilder syndrome --\nSchindler disease --\nSchinzel syndrome --\nSchinzel-giedion syndrome --\nSchinzel acrocallosal syndrome --\nScholz-greenfield syndrome --\nSchönlein-henoch purpura syndrome --\nSchopf-schulz-passarge syndrome --\nSchwartz-jampel syndrome --\nScids (severe combined immunodeficient syndrome) --\nSclerema neonatorum --\nScurvy syndrome --\nSea-blue histiocytosis syndrome --\nSegawa syndrome --\nSeitelberger syndrome --\nSenear-usher syndrome --\nSengers syndrome --\nSensenbrenner syndrome --\nSerpentine fibula-polycystic kidney syndrome --\nSetleis syndrome --\nSheehan syndrome --\nShokeir syndrome --\nShone complex or syndrome --\nShort-rib polysyndactyly syndrome --\nShort syndrome --\nShwachman syndrome --\nShy-drager syndrome --\nSimmonds syndrome --\nSimpson-golabi-behmel syndrome --\nSingleton-merten syndrome --\nSitus inversus --\nSjögren larsson syndrome (sls) --\nSneddon syndrome --\nSpastic diplegia of infancy --\nSpinal muscular atrophy syndrome --\nSpinocerebellar ataxia (sca): an overview --\nSponastrime dysplasia --\nSpondylocarpotarsal synostosis syndrome --\nSpondyloepimetaphyseal dysplasia --\nStargardt syndrome --\nStein-leventhal syndrome --\nStiff baby syndrome --\nStiff heart syndrome --\nStimmler syndrome --\nStreeter anomaly --\nSuccinyl-coa:3-ketoacid coa-transferase deficiency --\nSummerskill syndrome --\nSuperior mesenteric artery syndrome (smas) --\nSwyer syndrome. Swyer-james-macleod syndrome --\nSylvian syndrome --\nTakayasu disease --\nTangier disease --\nTel hashomer camptodactyly syndrome --\nTemtamy syndrome --\nThanatophoric dwarfism --\nThanos-stewart-zonana syndrome --\nThree m syndrome --\nThrombotic thrombocytopenic purpura (ttp) --\nThyrotoxic periodic paralysis --\nTooth and nail syndrome --\nTorch syndrome --\nToriello-carey syndrome --\nTriad anomaly --\nTricho-dento-osseous (tdo) syndrome --\nTricho-oculo-dermo-vertebral syndrome (todv syndrome) --\nTricho-rhino-phalangeal dysplasia type i --\nTricho-rhino-phalangeal dysplasia type ii --\nTricho-rhino-phalangeal dysplasia type iii --\nTriglyceride storage disease (tsd) --\nTrimethylaminuria syndrome --\nTrisomy 3p --\nTrisomy 4p --\nTrisomy 6q --\nTrisomy 8 --\nTrisomy 11q --\nTrisomy 13 --\nTrisomy 18 --\nTrisomy 21 --\nTruncus arteriosus communis --\nTurcot syndrome --\nUhl anomaly --\nUllrich disease --\nUllrich-feichtiger syndrome --\nUllrich-turner syndrome --\nUpshaw-schulman syndrome --\nUrbach-wiethe syndrome --\nUridine diphosphate galactose epimerase deficiency --\nUrticaria pigmentosa --\nVacterl association with hydrocephalus --\nVa(c)ter(l) association --\nVan maldergem wetzburger verloes syndrome --\nVaquez-osler disease --\nVaradi-papp syndrome --\nVasquez hurst sotos syndrome --\nVelo-facio-skeletal syndrome --\nVerner-morrison syndrome --\nVogt-koyanagi-harada syndrome --\nVohwinkel syndrome --\nVon gierke disease --\nVon hippel lindau syndrome --\nVon willebrand-jüergens disease --\nWadia-swami syndrome --\nWagner syndrome --\nWaterhouse-friderichsen syndrome --\nWatson syndrome --\nWeaver syndrome --\nWeber-christian disease --\nWeismann-netter-stuhl syndrome --\nWermer syndrome --\nWerner syndrome --\nWest syndrome --\nWeyers syndrome ii --\nWiedemann-rautenstrauch syndrome --\nWilliams-campbell syndrome --\nWilson-turner syndrome --\nWohlfart-kugelberg-welander syndrome --\nWolff-parkinson-white (wpw) syndrome --\nWyburn mason syndrome --\nXeroderma pigmentosum (xp) --\nXeroderma, talipes, and enamel defect syndrome --\nX-linked adrenoleukodystrophy (xla) --\nX-linked hypophosphatemia (xlh) --\nX-linked lymphoproliferative (xlp) syndrome --\nYellow nail syndrome --\nYoung syndrome --\nYunis-varon syndrome --\nZunich neuroectodermal syndrome.\neditors, Bruno Bissonnette, Igor Luginbuehl, Bruno Marciniak, Bernard J. Dalens.\n<http://www.worldcat.org/oclc/607731405> # Syndromes : rapid recognition and perioperative implications\nlibrary:oclcnum "607731405" ;\nschema:description "L-2-hydroxyglutaric aciduria -- Laband syndrome -- Lacrimo-auriculo-dento-digital syndrome (ladd syndrome) -- Lafora syndrome or disease -- Lambert syndrome -- Landau-kleffner syndrome (lks) -- Landouzy-dejerine dystrophy -- Laron syndrome -- Larsen syndrome -- Laryngo-onycho-cutaneous (loc) syndrome -- Launois syndrome -- Laurence moon syndrome (lms) -- Leber congenital amaurosis (lca) -- Leber hereditary optic neuropathy (lhon) -- Legg-calvé-perthes disease -- Leigh syndrome -- Leiner syndrome -- Lemierre syndrome -- Lennox-gastaut syndrome -- Lenz syndrome -- Lenz-majewski syndrome -- Leopard syndrome -- Leri pleonosteosis -- Léri-weill syndrome -- Lesch-nyhan syndrome -- Letterer-siwe disease (lsd) -- Leukocyte adhesion deficiency (lad) syndrome -- Leukodystrophies: overview -- Leukonychia and other nail discoloration: overview -- Leukonychia totalis -- Liddle syndrome -- Li-fraumeni syndrome (lfs) -- Lightwood syndrome -- Limb deficiency-heart malformation syndrome -- Limb-girdle muscular dystrophy (lgmd) -- Lipofuscinoses, neuronal ceroid: overview -- Lissencephaly -- Loken senior syndrome -- Long qt syndrome (lqts) -- Louis-bar syndrome -- Lowe syndrome -- Lown-ganong-levine syndrome -- Lowry-wood syndrome -- Lucey-driscoll syndrome -- Lujan fryns syndrome -- Lutembacher syndrome -- Lyell syndrome -- Lyme disease -- Lymphedema -- Lymphedema hypoparathyroidism syndrome -- Lymphedema with distichiasis -- Lymphoreticular syndrome -- Lynch syndrome -- Lysinuric protein intolerance -- Machado-joseph disease -- Macrocephaly, hypertelorism, short limbs, and hearing loss syndrome -- Maffucci syndrome -- Majocchi disease -- Mallory-weiss syndrome -- Malpuech syndrome -- Mannosidosis -- Maple syrup urine disease (msud) -- Marden-walker syndrome -- Marfan syndrome -- Marinesco-sjögren syndrome -- Maroteaux cohen-solal bonaventure syndrome -- Maroteaux-lamy syndrome -- Marshall syndrome -- Marshall-smith syndrome -- Masa syndrome -- Mastocytosis -- Mauriac syndrome -- Mayer-von rokitansky-küster-hauser syndrome -- Mccune-albright syndrome -- Mckusick-kaufman syndrome -- Mcpherson-clemens syndrome -- Meckel-gruber syndrome (mks) -- Median cleft facial syndrome -- Meier-gorlin syndrome -- Meigs syndrome (including pseudo-meigs syndrome) -- Melanoma-astrocytoma syndrome -- Melas syndrome -- Melkersson-rosenthal syndrome -- Melnick-fraser syndrome -- Melnick-needles syndrome (mns) -- Meltzer syndrome -- Menkes syndrome -- Meretoja syndrome -- Merlob syndrome -- Merrf syndrome -- Mesomelia-synostoses syndrome -- Metachromatic leukodystrophy -- Metaphyseal chondrodysplasia, jansen type -- Metaphyseal chondrodysplasia, mckusick type -- Metaphyseal chondrodysplasia, schmid type -- Methemoglobinemia (congenital) -- Methionine malabsorption syndrome -- Methylmalonic acidemia (mma) -- Meyer-betz disease -- Michels syndrome -- Microgastria-limb reduction defects association -- Microvillous inclusion syndrome -- Macrocephaly, hypertelorism, short limbs, and hearing loss syndrome -- Maffucci syndrome -- Majocchi disease -- Mallory-weiss syndrome -- Malpuech syndrome -- Mannosidosis -- Maple syrup urine disease (msud) -- Marden-walker syndrome -- Marfan syndrome -- Marinesco-sjögren syndrome -- Maroteaux cohen-solal bonaventure syndrome -- Maroteaux-lamy syndrome -- Marshall syndrome -- Marshall-smith syndrome -- Masa syndrome -- Mastocytosis -- Mauriac syndrome -- Mayer-von rokitansky-küster-hauser syndrome -- Mccune-albright syndrome -- Mckusick-kaufman syndrome -- Mcpherson-clemens syndrome -- Meckel-gruber syndrome (mks) -- Median cleft facial syndrome -- Meier-gorlin syndrome -- Meigs syndrome (including pseudo-meigs syndrome) -- Melanoma-astrocytoma syndrome."@en ;\nschema:description "Gianotti-crosti syndrome -- Gilbert syndrome -- Gilles de la tourette syndrome -- Gillespie syndrome -- Gitelman syndrome -- Glanzmann thrombasthenia -- Glucose-6-phosphate dehydrogenase deficiency -- Glucose phosphate isomerase deficiency -- Glutaric acidemia type i (ga-i) -- Glutaric acidemia type ii (ga-ii) -- Glycogen storage diseases (gsd): an overview -- Glycogen storage disease type 0 -- Glycogen storage disease type i (gsd i) -- Glycogen storage disease type ii -- Glycogen storage disease type iii (gsd iii) -- Glycogen storage disease type iv (gsd iv) -- Glycogen storage disease type v (gsd v) -- Glycogen storage disease type vi (gsd vi) -- Glycogen storage disease type vii (gsd vii) -- Glycogen storage disease type viii (gsd viii) -- Goldenhar syndrome -- Goldston syndrome -- Goltz syndrome -- Goodman camptodactyly -- Goodpasture syndrome -- Gordon-holmes syndrome -- Gordon hyperkalemia-hypertension syndrome -- Gorham-stout disease -- Gorlin-chaudry-moss syndrome -- Gorlin-goltz syndrome -- Gottron syndrome -- Gradenigo syndrome -- Graham-boyle-troxell syndrome -- Grand-kaine-fulling syndrome -- Granddad syndrome -- Grant syndrome -- Graves disease -- Greig cephalopolysyndactyly syndrome -- Griscelli syndrome -- Grisel syndrome -- Grix-blankenship-peterson syndrome -- Groenblad-strandberg syndrome -- Groll-hirschowitz syndrome -- Gsell-erdheim syndrome -- Guizar-vasquez-luengas syndrome -- Gullner syndrome -- Gunn syndrome -- Hageman factor (factor xii) deficiency -- Haim munk syndrome -- Hajdu cheney syndrome -- Hakim-adams syndrome -- Hall riggs syndrome -- Hallerman-streiff syndrome -- Hallervorden-spatz disease -- Haltia-santavuori syndrome -- Hanot-chauffard syndrome -- Happy puppet syndrome -- Harboyan syndrome -- Hard syndrome -- Hardcastle syndrome -- Harlequin syndrome -- Hartnup disease -- Hdr syndrome -- Hecht syndrome -- Hemochromatosis -- Hemoglobin disorders: overview -- Hemolytic anemia, congenital, with emphysema and cutis laxa -- Hemophagocytotic lymphohistiocytosis (hlh) -- Hemophilia a -- Hemophilia b -- Hennekam syndrome -- Hereditary acromelalgia -- Hereditary desmoid disease (hdd) -- Hereditary keratitis -- Hereditary motor sensory neuropathies (hmsn): overview -- Hereditary neurocutaneous angiomatoses: overview -- Hereditary neurocutaneous angioma -- Hereditary pancreatitis -- Hereditary sensory and autonomic neuropathies (hsan): overview -- Hereditary spherocytosis -- Hereditary stomatocytosis -- Hereditary telangiectasia -- Hereditary vitamin d-resistant rickets (hvdrr) -- Hereditary xerocytosis -- Hermansky-pudlak syndrome (hps) -- Hhh syndrome -- Hhhh syndrome -- Hirschsprung syndrome -- Histidinemia -- Histiocytosis -- Holt-oram syndrome -- Homocystinuria (hcu) -- Horton syndrome -- Hughes syndrome -- Hunter syndrome -- Huntington chorea (hc) -- Hurler syndrome -- Hypereosinophilic syndrome (hes) -- Hyperlipoproteinemia: an overview -- Hyperoxaluria, primary -- Hyperprolinemia -- Hypoglossia-hypodactylia syndrome -- Hypomelanosis of ito -- Hypoparathyroidism -- Hypophosphatasia -- Hypoplasia of the right ventricle -- Hypoplastic left heart syndrome -- Ice syndrome -- I-cell disease -- Ichthyosis vulgaris -- Idiopathic intracranial hypertension -- Idiopathic thrombocytopenia purpura -- Imerslund syndrome -- Iminoglycinuria -- Immotile cilia syndrome -- Immunodeficiency centromeric instability and facial anomalies syndrome -- Inclusion body myopathy -- Incontinentia pigmenti -- Infantile pyloric stenosis -- Infantile sialic acid storage disease -- Infantile-onset spinocerebellar ataxia (iosca) -- Infertile male syndrome -- Intestinal pseudoobstruction caused by neuronal disease -- Iridogoniodysgenesis syndrome -- Isaacs mertens syndrome -- Ischiopatellar dysplasia -- Isotretinoin embryopathy-like syndrome -- Isovaleric acidemia -- Ivemark syndrome -- Ivic syndrome -- Jacobs syndrome -- Jacobsen syndrome -- Jaffe-lichtenstein syndrome -- Jarcho-levin syndrome -- Jeune syndrome -- Job syndrome -- Johanson-blizzard syndrome (jbs) -- Johnson munson syndrome -- Jones syndrome -- Joubert syndrome -- Juberg-hayward syndrome -- Juberg-marsidi syndrome -- Judge misch wright syndrome -- Jumping frenchman of maine syndrome -- Jung wolff back stahl syndrome -- Juvenile hyaline fibromatosis -- Juvenile intestinal polyposis -- Juvenile myoclonic epilepsy (jme) -- Juvenile paralysis agitans of hunt."@en ;\nschema:description "Juvenile sulfatidosis syndrome -- Kabuki syndrome -- Kaler-garrity-stern syndrome -- Kallmann syndrome -- Kantaputra-gorlin syndrome -- Kaplowitz-bodurtha syndrome -- Kaposi sarcoma -- Kapur-toriello syndrome -- Karandikar-maria-kamble syndrome -- Karsch-neugebauer syndrome -- Kartagener syndrome -- Kasabach-merritt syndrome -- Kashani-strom-utley syndrome -- Kasznica-carlson-coppedge syndrome -- Katsantoni-papadakou-lagoyanni syndrome -- Katz syndrome -- Kaufman oculo-cerebro-facial syndrome -- Kaveggia syndrome -- Kawasaki disease -- Kawashima-tsuji syndrome -- Kbg syndrome -- Kearns-sayre syndrome -- Kennedy disease -- Kennerknecht-vogel syndrome -- Kenny-caffey syndrome -- Keratitis ichthyosis deafness (kid) syndrome -- Keratitis, hereditary -- Keratosis palmaris et plantaris: overview -- Keratosis palmoplantaris with esophageal cancer -- Kersey syndrome -- Ketoacidosis of infancy -- Keutel syndrome -- Khalifa-graham syndrome -- Kikuchi-fujimoto disease -- Kindler syndrome -- King-denborough syndrome -- Kinky hair syndrome -- Kinsbourne syndrome -- Kleine-levin hibernation syndrome -- Kleiner-holmes syndrome -- Klinefelter syndrome xxy/xyy -- Klippel-feil syndrome -- Klippel-trenaunay syndrome -- Kniest syndrome -- Knobloch syndrome -- Köbberling-dunnigan syndrome -- Kocher-debré-sémélaigne syndrome -- Konigsmark syndrome -- Korula-wilson-salomon syndrome -- Kostmann syndrome -- Kosztolanyi syndrome -- Kousseff-nichols syndrome -- Kousseff syndrome -- Kowarski syndrome -- Kozlowski-brown-hardwick syndrome -- Kozlowski-celermajer syndrome -- Kozlowski-ouvrier syndrome -- Kozlowski-rafinski-kucharska syndrome -- Kozlowski-tsuruta-taki syndrome -- Kozlowski-warren-fisher syndrome -- Krasnow-qazi syndrome -- Krause-kivlin syndrome -- Krause-reese syndrome -- Krauss-herman-holmes syndrome -- Krieble-bixler syndrome -- Kudo-tamura-fuse syndrome -- Kumar-levick syndrome -- Kunze-riehm syndrome -- Kurczynski-casperson syndrome -- Kuster-majewski-hammerstein syndrome -- Kuzniecky syndrome -- Kwashiorkor -- Kyrle disease."@en ;\nschema:description "Melas syndrome -- Melkersson-rosenthal syndrome -- Melnick-fraser syndrome -- Melnick-needles syndrome (mns) -- Meltzer syndrome -- Menkes syndrome -- Meretoja syndrome -- Merlob syndrome -- Merrf syndrome -- Mesomelia-synostoses syndrome -- Metachromatic leukodystrophy -- Metaphyseal chondrodysplasia, jansen type -- Metaphyseal chondrodysplasia, mckusick type -- Metaphyseal chondrodysplasia, schmid type -- Methemoglobinemia (congenital) -- Methionine malabsorption syndrome -- Methylmalonic acidemia (mma) -- Meyer-betz disease -- Michels syndrome -- Microgastria-limb reduction defects association -- Microvillous inclusion syndrome -- Midas syndrome -- Miller-dieker lissencephaly syndrome -- Miller disease -- Miller fisher syndrome -- Miller syndrome -- Milroy disease -- Milton disease -- Minicore disease with external ophthalmoplegia -- Mitochondrial acetoacetyl-coa thiolase (acat) deficiency -- Mitochondrial disease -- Moebius syndrome -- Mohr syndrome -- Mohr-tranebjaerg syndrome -- Mollica pavone antener syndrome -- Moloney syndrome -- Molybdenum cofactor deficiency -- Momo syndrome -- Monilethrix -- Moore-federman syndrome -- Moore-smith-weaver syndrome -- Morgagni-stewart-morel syndrome -- Morning glory syndrome -- Morquio syndrome -- Mount reback syndrome -- Mowat-wilson syndrome -- Moyamoya syndrome -- Moynahan alopecia syndrome -- Muckle-wells syndrome -- Mucolipidosis -- Mucopolysaccharidosis (mps) -- Mucoviscidosis -- Muir-torre syndrome (mts) -- Mulibrey nanism syndrome -- Muller barth menger syndrome -- Multicore myopathy -- Multiple carboxylase deficiency -- Multiple endocrine neoplasia (men) -- Multiple epiphyseal dysplasia (med) -- Multiple synostoses syndrome -- Murcs association -- Myasthenia gravis -- Myoadenylate deaminase deficiency -- Myocerebellar disorder -- Myopathy, distal, welander type -- Myotonia congenita -- Myotonic dystrophy -- Myotubular myopathy -- Myhre syndrome -- N syndrome -- N-acetylglutamate synthetase deficiency -- Nager syndrome -- Nail-patella syndrome -- Nance-horan syndrome -- Narp syndrome -- Nélaton syndrome -- Nemaline rod myopathy -- Neonatal lupus erythematosus -- Netherton syndrome -- Neurocutaneous melanosis -- Neurofibromatosis generalisata -- Neuronal ceroid lipofuscinoses -- Nezelof syndrome -- Niemann-pick disease -- Nonketotic hyperglycinemia -- Noonan syndrome -- Norrie disease -- Nyssen-van bogaert syndrome -- Oculocerebral with hypopigmentation syndrome -- Oculodentodigital syndrome -- Oculogastrointestinal muscular dystrophy -- Odontotrichomelic syndrome -- Ogilvie syndrome -- Omenn syndrome -- Omodysplasia -- Ondine syndrome -- Opitz-frias syndrome -- Oral-facial-digital syndrome (ofd) -- Ornithine carbamoyltransferase deficiency (otcd) -- Ornithine delta-aminotransferase deficiency -- Orotic aciduria -- Osgood-schlatter disease -- Osteogenesis imperfecta -- Osteopetrosis -- Otopalatodigital (opd) syndrome type i -- Otopalatodigital (opd) syndrome type ii -- Otospondylomegaepiphyseal dysplasia -- Pachydermoperiostosis (pdp) -- Pagod syndrome -- Pallister-hall syndrome -- Papillon-lefèvre syndrome -- Parana hard skin syndrome -- Paroxysmal cold hemoglobinuria -- Paroxysmal nocturnal hemolytic (pnh) anemia -- Parry-romberg syndrome -- Patterson pseudo-leprechaunism syndrome -- Pearson syndrome -- Pectus excavatum -- Pelizaeus-merzbacher syndrome -- Pemphigoid -- Pemphigus -- Pena-shokeir syndrome type i -- Pena-shokeir syndrome type ii -- Pendred syndrome -- Penta x syndrome -- Pentalogy of cantrell -- Pentosuria -- Pep syndrome -- Periodic paralysis (pp) -- Perlman syndrome -- Pernicious anemia -- Perrault syndrome -- Pettigrew syndrome -- Peutz-jeghers syndrome -- Phace syndrome -- Phenylketonuria -- Pheochromocytoma -- Phosphoenolpyruvate carboxykinase deficiency -- Phosphoglycerate kinase deficiency -- Phytosterolemia -- Pickwickian syndrome -- Pierre robin syndrome -- Pilomatrixoma -- Pitt-rogers-danks syndrome -- Pitt-williams brachydactyly syndrome -- Pituitary dwarfism -- Plott syndrome -- Poland syndrome -- Poland-moebius syndrome -- Polip syndrome -- Pollitt syndrome -- Polyarteritis nodosa (pan) -- Polycystic kidney disease (pkd) -- Polycystic liver disease -- Polyostotic osteolytic dysplasia -- Porokeratosis of mibelli -- Porphyrias -- Potter syndrome -- Powell venencie gordon syndrome -- Prader-labhart-willi syndrome -- Precocious puberty -- Primary immunodeficiencies -- Primary pulmonary hypertension (pph) -- Primary torsion dystonia -- Progeria syndrome -- Progressive bulbar palsy of childhood -- Progressive familial intrahepatic cholestasis (pfic) -- Prolidase deficiency -- Propionic acidemia -- Protein c deficiency -- Protein s deficiency -- Proteus syndrome -- Proximal muscular dystrophy -- Prune belly syndrome -- Psaume syndrome -- Pseudo-achondroplastic dysplasia -- Pseudohypoparathyroidism -- Pterygium syndrome -- Pulmonary alveolar microlithiasis -- Pulmonary alveolar proteinosis -- Pulmonary arteriovenous malformation -- Pulmonary hypoplasia -- Purine nucleoside phosphorylase deficiency -- Purtscher disease -- Pyknodysostosis -- Pyle disease -- Pyruvate carboxylase deficiency -- Pyruvate dehydrogenase complex deficiency -- Pyruvate kinase deficiency (pkd)."@en ;\nschema:description "Blue diaper syndrome -- Blue rubber bleb nevus syndrome -- Book syndrome -- Boomerang dysplasia -- Börjeson-forssman-lehmann syndrome -- Borrone dermato-cardio-skeletal syndrome -- Boucher-neuhäuser syndrome -- Bouveret syndrome -- Bowen syndrome -- Bowen-conradi syndrome -- Brachmann-de lange syndrome -- Brachydactyly-ectrodactyly syndrome with fibular aplasia or hypoplasia -- Brachymorphism-onychodysplasia-dysphalangism syndrome -- Branchial myoclonus with spastic paraparesis and cerebellar ataxia syndrome -- Branchio-oculo-facial syndrome -- Branchio-skeleto-genital syndrome -- Brauer syndrome -- Brittle hair and mental deficit syndrome -- Bronze baby syndrome -- Brown-vialetto-van laere syndrome -- Brugada syndrome -- Bruyn-scheltens syndrome -- Budd-chiari syndrome -- Burton syndrome -- Buschke-ollendorff syndrome -- Wagr syndrome -- Brunner winter syndrome -- C syndrome -- Cacchi-ricci disease -- Cadasil -- Cahmr syndrome -- Calderon gonzalez-cantu syndrome -- Camfak syndrome -- Camptodactyly syndrome, guadalajara types i and ii -- Camurati-engelmann syndrome -- Canavan syndrome -- Cantalamessa-baldiniambrosi syndrome -- Cantu syndrome -- Capos syndrome -- Carbon baby syndrome -- Cardiogenital syndrome -- Carey-fineman-ziter syndrome -- Carmi syndrome -- Carnevale-canun-mendoza syndrome -- Carnevale-hernandez-castillotorres syndrome -- Carnevale-krajewska-fischetto syndrome -- Carney complex -- Carnitine deficiency -- Carnitine palmitoyltransferase deficiency -- Carnosinemia -- Caroli disease and caroli syndrome -- Carpal tunnel syndrome -- Cartilage-hair hypoplasia syndrome -- Cartwright-nelson-fryns syndrome -- Castleman disease -- Castro-gago-pombonovo syndrome -- Cat cry syndrome -- Cat eye syndrome -- Cataract-alopecia-sclerodactyly syndrome -- Cataract-microcornea-syndrome -- Catlin marks -- Cavernous sinus syndrome -- Cayler syndrome -- Ccge syndrome -- Cecato-de lima-pinheiro syndrome -- Celiac disease -- Cenani syndactylism -- Cennamo gangemi magli syndrome -- Central core disease -- Cephaloskeletal dysplasia -- Cerebellar hypoplasia -- Cerebral aneurysm-cirrhosis syndrome -- Cerebro-oculo-skeleto-renal syndrome -- Cerebro-reno-digital syndrome -- Cerebrocortical degeneration of infancy -- Cerebrocostomandibular syndrome -- Ceroid storage disease -- Ceruloplasmin deficiency -- Cervico-oculo-acoustic syndrome -- Chands -- Charcot-marie-tooth disease -- Charge syndrome -- Charlie m syndrome -- Chauffard syndrome -- Chediak-higashi syndrome -- Chemke-oliver-mallek syndrome -- Cherubism -- Child syndrome -- Cholinesterase deficiency -- Chondrodysplasia giant cell type -- Chondrodysplasia grebe type -- Chondrodysplasia-pseudohermaphroditism syndrome -- Chondrodysplasia punctata -- Chorioretinal dysplasia-microcephaly-mental retardation syndrome -- Choroideremia -- Christ-siemens-touraine syndrome -- Chronic fatigue syndrome -- Chronic granulomatous disease -- Chudley mental retardation syndrome -- Chudley-rozdilsky-houston syndrome -- Citrullinemia -- Cleft hand and absent tibia syndrome -- Cleft-limb-heart malformation syndrome -- Cleft palate lateral synechiae syndrome -- Cleidocranial dysplasia -- Cleidorhizomelic syndrome -- Cloverleaf skull -- Clubfoot -- Coach syndrome -- Coats disease -- Cockayne syndrome -- Codas syndrome -- Coffin-lowry syndrome -- Coffin-siris syndrome -- Cohen syndrome -- Cold agglutinin syndrome -- Cold hypersensitivity syndrome -- Cole-carpenter syndrome -- Coleman-randall syndrome -- Collins-dennis-clarke-pope syndrome -- Collodion baby -- Colpocephaly -- Complete androgen insensitivity syndrome -- Complex disease/deficiency (overview) -- Complex i deficiency -- Complex ii deficiency -- Complex iii deficiency -- Complex iv deficiency -- Complex v deficiency -- Cone-rod retinal dystrophies -- Congenital afibrinogenemia -- Congenital atresia of larynx -- Congenital disorders of glycosylation -- Congenital dyserythropoietic anemias -- Congenital factor vii deficiency -- Congenital hypothyroidism -- Congenital muscular dystrophy: an overview -- Congenital myopathy with fiber-type disproportion -- Congenital pancreatic agenesis -- Congenital pseudarthrosis of clavicle -- Congenital pulmonary hypoplasia -- Congenital shortness of the costocoracoid ligament -- Congenital stridor -- Congenital varicella syndrome -- Conn syndrome -- Cooks syndrome -- Corneal cerebellar syndrome -- Corneodermatoosseous syndrome -- Corpus callosum agenesis -- Costello syndrome -- Cousin-walbaum-cegarra syndrome -- Cowchock syndrome -- Cowden syndrome -- Cramer-niederdellmann syndrome -- Crane-heise syndrome -- Craniodiaphyseal dysplasia -- Craniofrontonasal dysplasia -- Craniolacunia -- Craniomicromelic syndrome -- Craniosynostosis -- Crest syndrome -- Creutzfeldt-jakob disease -- Crigler-najjar syndrome -- Cumming syndrome -- Curatolo-cilio syndrome -- Cutis laxa -- Cutis marmorata telangiectatica congenita -- Cystic hygroma -- Cystinosis."@en ;\nschema:description "Qazi markouizos syndrome -- (de) quervain thyroiditis -- Quincke edema -- Rabson-mendenhall syndrome -- Radial aplasia syndrome -- Radio-ulnar synostosis -- Ramban-hasharon syndrome -- Ramon syndrome -- Ramsay hunt syndrome type i -- Ramsay hunt syndrome type ii -- Raynaud syndrome -- Rear syndrome -- Reardon wilson cavanagh syndrome -- Recombinant chromosome 8 syndrome -- Refetoff syndrome -- Refsum syndrome -- Reifenstein syndrome -- Renal-coloboma syndrome -- Renal tubular dysgenesis -- Reticular dysgenesia -- Retinoblastoma -- Retino-hepato-endocrinologic syndrome -- Rett syndrome -- Reye syndrome -- Reynolds neri hermann syndrome -- Rhizomelic chondrodysplasia punctata type i -- Richards rundle syndrome -- Riley-smith syndrome -- Ritscher-schinzel syndrome -- Roberts syndrome -- Robinow syndrome -- Rogers syndrome -- Rolland-desbuquois syndrome -- Rombo syndrome -- Rosenberg-chutorian syndrome -- Rosenthal-kloepfer syndrome -- Rosewater syndrome -- Rosseli-gulienetti syndrome -- Rothmann makai syndrome -- Rothmund-thomson syndrome -- Rotor syndrome -- Roussy-levy syndrome -- Rubinstein-taybi syndrome -- Rud syndrome -- Rukavina type amyloid polyneuropathy -- Rundles-falls syndrome -- Russell weaver bull syndrome -- Russell-silver syndrome -- Rutledge lethal multiple congenital anomaly syndrome -- Ruvalcaba syndrome -- Sabin-feldman syndrome -- Salt-depletion syndrome -- Sandifer syndrome -- Sandrow syndrome -- Sanjad-sakati syndrome -- Sarcoidosis -- Sarcosinemia -- Sc phocomelia syndrome -- Schilder syndrome -- Schindler disease -- Schinzel syndrome -- Schinzel-giedion syndrome -- Schinzel acrocallosal syndrome -- Scholz-greenfield syndrome -- Schönlein-henoch purpura syndrome -- Schopf-schulz-passarge syndrome -- Schwartz-jampel syndrome -- Scids (severe combined immunodeficient syndrome) -- Scimitar syndrome -- Sclerema neonatorum -- Scurvy syndrome -- Sea-blue histiocytosis syndrome -- Seckel syndrome -- Segawa syndrome -- Seitelberger syndrome -- Senear-usher syndrome -- Sengers syndrome -- Sensenbrenner syndrome -- Serpentine fibula-polycystic kidney syndrome -- Setleis syndrome -- Sheehan syndrome -- Shokeir syndrome -- Shone complex or syndrome -- Short-rib polysyndactyly syndrome -- Short syndrome -- Shwachman syndrome -- Shy-drager syndrome -- Siadh -- Sialidosis -- Sick sinus syndrome -- Sickle cell anemia -- Simmonds syndrome -- Simpson-golabi-behmel syndrome -- Singleton-merten syndrome -- Sirenomelia -- Situs inversus -- Sjögren larsson syndrome (sls) -- Sjögren syndrome -- Smith-lemli-opitz syndrome -- Smith-magenis syndrome -- Sneddon syndrome -- Sotos syndrome -- Spastic diplegia of infancy -- Spina bifida -- Spinal muscular atrophy syndrome -- Spinocerebellar ataxia (sca): an overview -- Sponastrime dysplasia -- Spondylocarpotarsal synostosis syndrome -- Spondylo-enchondro-dysplasia -- Spondyloepimetaphyseal dysplasia -- Stargardt syndrome -- Stein-leventhal syndrome -- Stickler syndrome -- Stiff baby syndrome -- Stiff heart syndrome -- Stimmler syndrome -- Streeter anomaly -- Sturge-weber syndrome -- Succinyl-coa:3-ketoacid coa-transferase deficiency -- Sudden infant death syndrome (sids) -- Sulfocysteinuria -- Summerskill syndrome -- Superior mesenteric artery syndrome (smas) -- Sweet syndrome -- Swyer syndrome."@en ;\nschema:description "D-2-hydroxyglutaric aciduria -- Da silva syndrome -- Danbolt-closs syndrome -- Dandy-walker malformation -- Darier-white disease -- De die smulders vles fryns syndrome -- De morsier syndrome -- De sanctis cacchione syndrome -- De toni debré fanconi syndrome -- Deafness-optic atrophy syndrome -- Degos syndrome -- Dejerine-sottas syndrome -- Delleman oorthuys syndrome -- Dent disease -- Denys-drash syndrome -- Dermatomyositis and polymyositis -- Desbuquois syndrome -- Devriendt legius fryns syndrome -- D-glyceric acidemia -- Diaminopentanuria -- Diastematomyelia -- Diastrophic dysplasia -- Diencephalic syndrome -- Diferrante syndrome -- Digeorge syndrome -- Digitotalar dysmorphism -- Dihydropyrimidinase deficiency -- Dihydropyrimidine dehydrogenase deficiency -- Dionisi vici sabetta gambarara syndrome -- Disaccharide intolerance type i -- Disaccharide intolerance type ii -- Donnai-barrow syndrome -- Donohue syndrome -- Door syndrome -- Drachtman weinblatt sitarz syndrome -- Du pan syndrome -- Duane retraction syndrome -- Dubin-johnson syndrome -- Dubowitz syndrome -- Duchenne muscular dystrophy -- Duker weiss siber syndrome -- Dyggve-melchior-clausen syndrome -- Dyke-davidoff-masson syndrome -- Dyskeratosis congenita -- Dysosteosclerosis -- Dysplasia epiphysealis hemimelica -- Eastman-bixler syndrome -- Ebstein syndrome -- Ectodermal dysplasia -- Ectodermal dysplasia, ectrodactyly, and macular dystrophy (eem) syndrome -- Ectrodactyly -- Ectrodactyly, ectodermal dysplasia, and clefting (eec) syndrome -- Ehlers-danlos syndrome (eds): an overview -- Ehlers-danlos syndrome (eds) -- Eisenmenger reaction -- Elejalde syndrome -- Ellis-van creveld syndrome -- Emery-dreifuss muscular dystrophy (edmd) -- Encephalocele -- Eosinophilic endomyocardial disease -- Epidermal nevus syndrome -- Epidermolysis bullosa -- Epstein syndrome -- Erb and klumpke palsy -- Erdheim-chester disease (ecd) -- Eronen syndrome -- Erythema multiforme (em) -- Erythromelalgia -- Erythropoietic protoporphyria -- Essential thrombocythemia -- F syndrome -- Fabry disease -- Facio-oculo-acoustico-renal (foar) syndrome -- Facio-thoraco-genital syndrome -- Fahr syndrome -- Familial amyotrophic dystonic paraplegia -- Familial atrial myxoma -- Familial benign copper deficiency -- Familial generalized anhidrosis -- Familial hyperaldosteronism -- Familial hyperlysinemia -- Familial hypogonadotrophic eunuchoidism -- Familial inverted choreoathetosis -- Familial juvenile nephronophthisis (nph) -- Familial mediterranean fever -- Familial nonchromaffin paragangliomas -- Familial osteodysplasia -- Familial porencephaly -- Familial progressive scleroderma -- Fanconi anemia -- Fanconi-bickel syndrome (fbs) -- Farber uzman syndrome -- Faulk epstein jones syndrome -- Feigenbaum bergeron richardson syndrome -- Feingold syndrome -- Felty syndrome -- Femoral-facial syndrome -- Femur-fibula-ulna syndrome -- Fenton wilkinson toselano syndrome -- Fetal alcohol syndrome (fas) -- Fetal aminopterin syndrome -- Fetal cocaine syndrome -- Fg syndrome -- Fibrin stabilizing factor (factor xiii) deficiency -- Fibrocystic pulmonary dysplasia -- Fibrodysplasia ossificans progressiva -- Fibromatoses -- Floating-harbor syndrome (fhs) -- Foix alajouanine syndrome -- Folic acid deficiency -- Forsius-ericksson syndrome -- Fragile x syndrome -- Fraser syndrome -- Freeman-sheldon syndrome (fss) -- Friedreich ataxia (frda) -- Fronto-metaphyseal dysplasia of gorlin (fmd) -- Frydman cohen karmon syndrome -- Fryns syndrome -- Fucosidosis -- Galactosemia -- Galactosialidosis -- Gangliosidosis (gm1) type i -- Gangliosidosis (gm2) type ii -- Garcia-lurie syndrome -- Gaucher disease -- Geleophysic dysplasia -- Generalized arterial calcification of infancy -- Genoa syndrome -- Geroderma osteodysplastica syndrome -- Gerstmann-sträussler disease."@en ;\nschema:description "Swyer-james-macleod syndrome -- Sylvian syndrome -- Syringomyelia -- Systemic lupus erythematosus (sle) -- Takayasu disease -- Tangier disease -- Tar syndrome -- Tel hashomer camptodactyly syndrome -- Temtamy syndrome -- Tethered spinal cord syndrome -- Tetralogy of fallot -- Thalassemia -- Thanatophoric dwarfism -- Thanos-stewart-zonana syndrome -- Three m syndrome -- Thrombotic thrombocytopenic purpura (ttp) -- Thyrotoxic periodic paralysis -- Tooth and nail syndrome -- Torch syndrome -- Toriello-carey syndrome -- Treacher collins syndrome -- Triad anomaly -- Tricho-dento-osseous (tdo) syndrome -- Tricho-oculo-dermo-vertebral syndrome (todv syndrome) -- Tricho-rhino-phalangeal dysplasia type i -- Tricho-rhino-phalangeal dysplasia type ii -- Tricho-rhino-phalangeal dysplasia type iii -- Triglyceride storage disease (tsd) -- Trimethylaminuria syndrome -- Trisomy 3p -- Trisomy 4p -- Trisomy 6q -- Trisomy 8 -- Trisomy 9 -- Trisomy 11q -- Trisomy 13 -- Trisomy 18 -- Trisomy 21 -- Truncus arteriosus communis -- Tuberous sclerosis -- Turcot syndrome -- Tyrosinemia -- Uhl anomaly -- Ullrich disease -- Ullrich-feichtiger syndrome -- Ullrich-turner syndrome -- Upshaw-schulman syndrome -- Urbach-wiethe syndrome -- Uridine diphosphate galactose epimerase deficiency -- Urticaria pigmentosa -- Usher syndrome -- Vacterl association with hydrocephalus -- Va(c)ter(l) association -- Van der woude syndrome -- Van maldergem wetzburger verloes syndrome -- Vaquez-osler disease -- Varadi-papp syndrome -- Vasquez hurst sotos syndrome -- Velocardiofacial syndrome -- Velo-facio-skeletal syndrome -- Verner-morrison syndrome -- Vogt-koyanagi-harada syndrome -- Vohwinkel syndrome -- Von gierke disease -- Von hippel lindau syndrome -- Von willebrand-jüergens disease -- Waardenburg syndrome -- Wadia-swami syndrome -- Wagner syndrome -- Wagr syndrome -- Waterhouse-friderichsen syndrome -- Watson syndrome -- Weaver syndrome -- Weber-christian disease -- Weill-marchesani syndrome -- Weismann-netter-stuhl syndrome -- Wermer syndrome -- Werner syndrome -- West syndrome -- Weyers syndrome ii -- Whipple disease -- Wiedemann-rautenstrauch syndrome -- Williams syndrome -- Williams-campbell syndrome -- Wilson disease -- Wilson-turner syndrome -- Wiskott-aldrich syndrome -- Wohlfart-kugelberg-welander syndrome -- Wolff-parkinson-white (wpw) syndrome -- Wolf-hirschhorn syndrome -- Wolfram syndrome -- Wyburn mason syndrome -- Xanthinuria -- Xeroderma pigmentosum (xp) -- Xeroderma, talipes, and enamel defect syndrome -- X-linked adrenoleukodystrophy (xla) -- X-linked hypophosphatemia (xlh) -- X-linked lymphoproliferative (xlp) syndrome -- Yellow nail syndrome -- Young syndrome -- Yunis-varon syndrome -- Zellweger syndrome -- Zunich neuroectodermal syndrome."@en ;\nschema:isSimilarTo <http://www.worldcat.org/oclc/59003623> ;\nschema:productID "607731405" ;\nschema:publication <http://www.worldcat.org/title/-/oclc/607731405#PublicationEvent/new_york_mcgraw_hill_2006> ;\nschema:url <http://www.accessanesthesiology.com/resource/602> ;\nschema:url <http://accessanesthesiology.mhmedical.com/book.aspx?bookid=412> ;\nschema:url <http://books.google.com/books?id=koNqAAAAMAAJ> ;\nschema:url <http://catalog.hathitrust.org/api/volumes/oclc/59003623.html> ;\nwdrs:describedby <http://www.worldcat.org/title/-/oclc/607731405> ;\nschema:isSimilarTo <http://www.worldcat.org/oclc/607731405> ; # Syndromes : rapid recognition and perioperative implications\nschema:about <http://www.worldcat.org/oclc/607731405> ; # Syndromes : rapid recognition and perioperative implications


Auteur Topic: Re: Marceltal, CS2 Stall (gelezen 38474 keer)\nnevenspoor nveau 140 Marcelthal.JPG (237.46 kB, 1329x642 - bekeken 185 keer.)\nMarceltal_Bellegem_01_03.tra (170.54 kB - gedownload 125 keer.)\nIMG_0285.jpg (26.53 kB, 320x240 - bekeken 2550 keer.)\nGWS, Dirk-Jan, JoBe, mardig23, h0_miessie en 1 andere waarderen dit bericht\nIMG_0292.jpg (76.48 kB, 640x480 - bekeken 2376 keer.)\nIMG_0295.jpg (85.24 kB, 640x480 - bekeken 2362 keer.)\nJoBe, mardig23, h0_miessie, jaap nieboer en GWS waarderen dit bericht\nIMG_0471.jpg (75.75 kB, 640x480 - bekeken 2121 keer.)


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