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Il portale delle Malattie Rare e della FMF
AVVISO
Gennaio 2005
I nuovi elenchi con i links aggiornati, delle malattie rare il cui nome inizia con la lettera W,
si trovano nelle seguenti pagine del sito dell'
Associazione Rete Malattie Rare
:
(da *** a ***) - Elenco Malattie Rare e genetiche *Lettera *
(da *** a ***) - Elenco Malattie Rare e genetiche *Lettera *
=========================================================================
=========================================================================
ultimi aggiornamenti
Elenco malattie rare e genetiche"lettera W"
© FMFPC è un sito ideato, realizzato ed aggiornato da
un malato
di
FMF (Febbre Mediterranea Familiare)
© FMFPC is a site conceived, realized and updated by a patient of FMF (Familial Mediterranean Fever)
aggiornato 07 febbraio 2004
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Anomalie Cromosomiche
* Nome italiano[Sinonimi]•Nome inglese[Synonyms]•Nome francese[Synonymes]•Nome spagnolo[Sinónimos]•{n.indice OMIM}•<Vedi
legenda
>
W
*
W Sindrome
•
W Syndrome[Pallister syndrome 1/Median cleft upper lip-mental retardation-pugilistic facies syndrome]
•
W syndrome[Pallister W, syndrome de]
••{
311450
}
*
Waaler Aarskog Sindrome di
•
Basal cell nevus Syndrome[BCNS/Nevoid basal cell carcinoma syndrome/NBCCS/Multiple basal cell nevi, odontogenic keratocystis, and skeletal anomalies/Fifth phacomatosis/Gorlin Syndrome/Gorlin-Goltz Syndrome/Hydrocephalus, costovertebral dysplasia, and Sprengel anomaly]
•
Waaler arskog syndrome de[Hydrocephalie dysplasie costovertebrale sprengel anomalie de]
•••{
109400
}
*
Waardenburg Sindrome di (denominazione generica)
[Distopia epicantale-albinismo-sordità percettiva /Sindrome di Klein-Waardenburg/Distopia canthia medialis lateroversa/Sindrome ptosi-epicanto]/
Waardenburg tipo 1 Sindrome di
/
Waardenburg tipo 2 Sindrome di
/
Waardenburg tipo 3 Sindrome di
/
Waardenburg tipo Pierpont
•
Waardenburg Syndrome
/
Waardenburg anophthalmia syndrome
/
Waardenburg recessive anophthalmia syndrome
/
Waardenburg syndrome 3
•
Waardenburg syndrome
/
type 1
/
type 2
/
type 3
/
type pierpont
•
Waardenburg, Síndrome de
•{}
*
Waardenburg-Shah Sindrome di[Waardenburg tipo 4 Sindrome di]
•
Waardenburg-Shah Syndrome/Waardenburg Syndrome, type IV; WS4/Waardenburg-Hirschsprung disease/Waardenburg Syndrome variant/Shah-Waardenburg Syndrome/Hirschsprung disease with pigmentary anomaly/(Waardenburg-Shah Syndrome, neurologic variant/Waardenburg-Shah Syndrome with demyelinating neuropathy and leukodystrophy)]
•
Waardenburg-Shah, syndrome de[Waardenburg type 4, syndrome de/(Hirschsprung-pigmentation anomalies)]
••{
277580
}
* Waardenburg Klein Sindrome di•••
Waardenburg Klein, Síndrome de [Waardenburg, Síndrome de/Van der Hoeve Halbertsma Waardenburg Gualdi, Síndrome de/Ptosis Epicantus, Síndrome de/Mende, Síndrome de/Klein Waardenburg, Síndrome de]
•{
193500
-
193510
-
600193
}
* Waelsch Sindrome di•••
Waelsch, Síndrome de[Reiter, Síndrome de/Ruhr, Síndrome de/Uretro Oculo Articular, Síndrome/Artritis Venérea/Poliartritis Entérica/Feissinger Leroy Reiter, Síndrome de/Conjuntivo Uretro Sinovial, Síndrome/Artritis Blenorrágica Idiopática/Artritis Uretrítica]
•{}
*
Wagner Malattia di
Sindrome di[Sindrome di Wagner-Unverricht/Polimiosite interstiziale/Polimiosite gregarina/Pseudotrichinosi]••
Wagner, maladie de
••{}
* Wagner Stickler Sindrome di•
Stickler Syndrome, vitreous type1[Stickler Syndrome, membranous vitreous type/Artroophthalmopathy, hereditary progressive/AOM/Stickler Syndrome, type I/STL1]
••
Wagner Stickler, Síndrome de [Stickler, Síndrome de/Cambios Epifisarios y Miopía Magna/Oftalmoartropatía/Weissenbacher Zweymuller, Síndrome de/Artro Oftalmopatía]
•{
108300
-
604481
-
184840
}
*
WAGR SINDROME DI
/
WAGR Sindrome
[Tumore di Wilms-aniridia-anomalie genitourinarie-ritardo mentale]•
WAGR Syndrome
/
Wilms tumor-aniridia syndrome
/
Wilms tumor-aniridia-genitourinary abnormalities-mental retardation triad
/
Wilms tumor-aniridia-gonadoblastoma-mental retardation (WAGR) syndrome, association
•
WAGR syndrome
•
WAGR, Síndrome de
{
194072
}•
D
*
Walbaum Titran Durieux Crepin Sindrome di
[Ipoplasia del perone displasia scapolo-pelvica agenesia del IV dito]••
Walbaum titran durieux crepin syndrome de[Hypoplasie du perone dysplasie scapulopelvienne absence du 5eme doigt]
••{}
*
Waldenstrom, macroglobulinemia di[Waldenström, macroglobulinemia di]
•Macroglobulinemia , Waldenstrom[WM]•••{
153600
}
*
WALDMANN, MALATTIA DI
/
Waldmann disease
[Linfangectasia intestinale/Paraproteinemia monoclonale IgM/Macroglobulinemia idiopatica o primaria/Macroglobulinemia emorragica/Porpora macroglobulinemiaca]•
Waldmann Disease[Dysproteinemia, Familial/Enteropathy, Hypercatabolic Protein-Losing/Familial Hypoproteinemia with Lymphangietatic Enteropathy/Hypoproteinemia, Idiopathic/Intestinal Lymphangiectasia/Intestinal Lymphangiectasis/Lymphangiectasia, Primary Intestinal/Lymphangiectasis, Primary Intestinal/Lymphangiectatic Protein-Losing Enteropathy/Lymphedema, Neonatal due to Exudative Enteropathy/Protein-Losing Enteropathy Secondary to Congestive Heart Failure]
•••{
152800
}
* Waldenstrom Sindrome di[Macroglobulinemia essenziale]•••
Waldenstrom, Síndrome de
•{}
* Waisman Sindrome di•
Waisman syndrome
/
Waisman syndrome
•••{}
* Waisman-Laxová Sindrome di•
Waisman-Laxová syndrome
/
Waisman-Laxová syndrome
•••{}
* Waldenström Malattia di•
Waldenstrom's Macroglobulinemia
•
Waldenström, maladie de
••{}
* Waldmann Malattia di•
Waldmann Disease[Dysproteinemia, Familial/Enteropathy, Hypercatabolic Protein-Losing/Familial Hypoproteinemia with Lymphangietatic Enteropathy/Hypoproteinemia, Idiopathic/Intestinal Lymphangiectasia/Intestinal Lymphangiectasis/Lymphangiectasia, Primary Intestinal/Lymphangiectasis, Primary Intestinal/Lymphangiectatic/Protein-Losing Enteropathy/Lymphedema, Neonatal due to Exudative Enteropathy/Protein-Losing Enteropathy Secondary to Congestive Heart Failure]
•••{}
* Walker-Clodius Sindrome di•
Walker-Clodius syndrome [ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome/Rüdiger syndrome 1/cleft lip-cleft palate-lobster claw deformity syndrome/ectrodactyly-cleft lip/palate syndrome/ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome/ectrodactyly-ectodermal dysplasia-cleft palate syndrome/lobster-claw with ectodermal defects syndrome/split hand-cleft lip/palate and ectodermal (SCE) dysplasia/split hand/feet syndrome]
•••{
129900
}
*
Walker Dyson Sindrome di
••
Walker dyson syndrome de
••{}
* Walker lissencefalia Sindrome di•
Walker lissencephaly syndrome
•••{}
*
WALKER-WARBURG SINDROME DI
/
Walker-Warburg Sindrome di
•
Walker Warburg Syndrome
/
Walker-Warburg syndrome (WWS)
•
Walker-Warburg syndrome
•
Walker Warburg, Síndrome de
•{
236670
}
* Walker-Clodius Sindrome di•
Walker-Clodius syndrome
•••{}
*
Wallis Cremin Beighton Sindrome di
••
Wallis cremin beighton syndrome de[Enchondromatose nanisme surdite]
••{}
Wallis Zieff Goldblatt sindrome di
•Cleidorhizomelic Syndrome•
Wallis zieff goldblatt syndrome de[Cleido rhizomelique syndrome]
••{
119650
}
* Warburg Sindrome di•
Warburg syndrome
•••{}
*
Warburg Sjo Fledelius Sindrome di
••
Warburg sjo fledelius syndrome
••{}
*
Warburg Thomsen Sindrome di
••
Warburg thomsen syndrome
••{}
*
Warburton Anyane Yeboa sindrome di
••
Warburton anyane yeboa syndrome de
••{}
* Warfarin embriopatia/
Warfarina, esposizione prenatale alla
•
warfarin embryopathy[fetal anticoagulant syndrome/DiSala syndrome/congenital warfarin syndrome/coumarin syndrome/fetal warfarin syndrome/heparin embryopathy/warfarin syndrome]
•••{}
* Warkany Sindrome 1/Tipo 2•
Warkany syndrome 1
/
Warkany syndrome 2
•••{}
*
Warman Mulliken Hayward Sindrome di
••
Warman mulliken hayward syndrome de
••{}
*
Warman Mulliken Sindrome di
••
Warman mulliken syndrome de[Craniosynostose forme dominante autosomique]
••{
123101
}
*
Watson Sindrome di
•
Watson Syndrome[Pulmonic stenosis with cafe-au-lait spots/Cafe-au-lait spots with pilmonic stenosis]
•
Watson, syndrome de[Sténose pulmonaire-taches café-au-lait]
••{
193520
}
* Watson-Miller Sindrome•
Watson syndrome[Alagille syndrome (AGS)/Alagille-Watson syndrome (AWS)/Watson-Miller syndrome/ arteriohepatic dysplasia (AHD)/cardiovertebral syndrome/cholestasis-peripheral pulmonary stenosis/hepatic ductular hypoplasia/hepatic ductular hypoplasia-multiple malformations syndrome/hepatofacioneurocardiovertebral syndrome/paucity of interlobular bile ducts (PILBD)]
•••{
118450
}
*
WEAVER SINDROME DI
/
Weaver Sindrome di
[WSS/Sindrome di Weaver-Smith]•
Weaver Syndrome
/
Weaver syndrome
/
Weaver-Smith syndrome
[WWS]•
Weaver like syndrome de
•
Weaver syndrome de
•
Weaver, Síndrome de
[Weaver Smith, Síndrome de]•{
277590
}
*
Weaver Johnson Sindrome di
••
Weaver johnson syndrome de
••{}
*
Weaver-like Sindrome
•Weaver like syndrome•
Weaver like syndrome••{}
Weaver Williams Sindrome di
•
Weaver-Williams syndrome
•
Weaver williams syndrome de
••{}
*
Weber-Christian, panniculite di
Sindrome di Malattia di [Panniculite nodulare febbrile recidivante/ Malattia di Pfeiffer-Weber-Christian/ Spondilopanniculite/ Panniculite nodulare febbrile non suppurattiva]•••
Weber Christian, Síndrome de
••{}
M
* Weber Sindrome di[Sindrome di Weber-Dimitri /Malattia di Sturge]•
Weber-Dimitri syndrome[Sturge-Weber syndrome/SWS/Dimitri disease/Jahnke syndrome/Kalischer syndrome/Lawford syndrome/Müller syndrome/Parkes Weber syndrome/Parkes Weber and Dimitri syndrome/Schirmer syndrome/Sturge disease/Sturge syndrome/Sturge-Kalischer-Weber syndrome/Sturge-Weber angiomatosis/Sturge-Weber anomalad/Sturge-Weber-Dimitri syndrome/Sturge-Weber-Krabbe syndrome/Sturge-Weber-Thoma syndrome/Weber syndrome/angioma capillare et venosum calcificans/angiomatosis encephalofacialis/angiomatosis meningoulofacialis/angiomatosis-oculo-orbito-thalamo-encephalic syndrome/cerebrocutaneous angiomatosis/cutaneocerebral angioma/ectoneurodermal hamartoma/encephalocraniofacial angiomatosis/encephalofacial angiomatosis/encephalofacial neuroangiomatosis/encephalotrigeminal angiomatosis/encephalotrigeminal syndrome/fourth phacomatosis/meningeal capillary angiomatosis/meningofacial angiomatosis/meningo-oculofacial angiomatosis/neuroangiomatosis encephalofacialis/neurocutaneous syndrome/neuroectodermal hamartoma/neuro-oculocutaneous angiomatosis/neuroretinoangiomatosis/nevoid amentia/trigemino-encephalo-angiomatosis]
•••{
185300
}
*
Webster Deming Sindrome di
[Cranio-fronto-nasale displasia di Poland anomalia]••
Webster deming syndrome
••{}
*
Wegener Malattia di
[Granulomatosi rinogena/Granulomatosi di Wegener/Granuloma a cellule giganti del tratto respiratorio/Sindrome arteritico-polmonare-nefropatica]••
Wegener, maladie de
•
Wegener, Síndrome de
•{}
*
Wegmann Jones Smith Sindrome di
••
Wegmann jones smith syndrome de
••{}
* Weil Sindrome di[Leptospirosi itterica/Spirochetosi ittero-emorragica/Malattia di Vasilev/Malattia di Mathieu/Malattia di Landouzy/Malattia di Fiedler/Ittero leptospirale]•
Weil Syndrome
•••{-}
*
WEILL-MARCHESANI SINDROME DI
/
Weill Marchesani Sindrome di
[Dismorfodistrofia mesodermale congenita]•
Weill Marchesani Syndrome
•
Weill marchesani syndrome de
•
Weill Marchesani, Síndrome de
[Esferofagia Braquimorfia, Síndrome de/Dismorfodistrofia Mesodérmica Congénita/Dismorfodistrofia Mesodérmica Tipo Braquimórfica Congénita]•{
277600
}
*
Weinstein Kliman Scully Sindrome di
••
Weinstein kliman scully syndrome
••{}
* Weir Mitchell Malattia di•••
Weir Mitchell, Enfermedad de
[Eritermalgia/Mitchell, Enfermedad de/Gerhardt, Enfermedad de/Eritromelalgia]•{}
*
Weismann Netter Stuhl Sindrome di
•
Weismann Netter Stuhl Syndrome
•
Weismann netter stuhl syndrome de
••{}
*
Weissenbacher Zweymuller Sindrome di
••
Weissenbacher zweymuller syndrome
••
Weissenbacher Zweymuller, Síndrome de [Stickler, Síndrome de/Wagner Stickler, Síndrome de/Cambios Epifisarios y Miopía Magna/Oftalmoartropatía/Artro Oftalmopatía]
•{
108300
-
604481
-
184840
}
*
Weleber Hecht Bigle Sindrome di
••
Weleber hecht bigley syndrome de
••{}
*
Wellesley Carman French Sindrome di
••
Wellesley carman french syndrome de
••{}
*
Wells Sindrome di
•
Wells Syndrome
•
Wells syndrome de
••{}
*
Wells Jankovic Sindrome di
••
Wells jankovic syndrome de
••{}
* Went Sindrome di•
Went syndrome
•••{}
*
WERDNIG-HOFFMAN MALATTIA DI SINDROME DI
/
Werdnig-Hoffman Malattia di
[Atrofia muscolare progressiva spinale infantile ereditaria/Emiatrofia spinale (o mielopatica) progressiva ereditaria/Amiotrofia centripeta/Atrofia di Hoffmann/Paralisi di Werdnig-Hoffman]•
Werdnig Hoffman Disease
•
Werdnig-Hoffman, maladie de
••{}•
M
*
Werdnig Hoffman tipo 1 fratture
••
Werdnig hoffman type 1 fractures
••{}
* Werlhof Malattia di[Trombocitopenia essenziale/Porpora trombocitopenica costituzionale/Porpora cronica trombocitoenica]•••
Werlhof, Enfermedad de
•{}
*
Wermer Sindrome di
[Adenomatosi endocrina multipla/Neoplasia endocrina multipla/MEN]••
Wermer, syndrome de
••{}
*
WERNER SINDROME DI
/
Werner Sindrome di
[Progeria dell'adulto/Progeria adultorum/Senilità prematura]•
Werner Syndrome
•
Werner, syndrome de
••{
277700
}
* Westphall Malattia di•
Hypokalemic periodic paralysis[HOKPP]
•
Westphall, maladie de[Paralysie périodique type 1, hypokaliémique]
••{
170400
}
*
WEST SINDROME DI
/
West Sindrome di
[Encefalopatia mioclonica infantile/Eclampsia nutans/Spasmo di flessione/"Salaam convulsion"/
Spasmo infantile con ritardo mentale
]•
West Syndrome
/
West syndrome (WS)
•
West, syndrome de
••{}
*
Westerhof Beemer Cormane Sindrome di
••
Westerhof beemer cormane syndrome de[Macules congenitales hypopigmentees hyperpigmentees]
••{
154000
}
*
Westphall Malattia di
[Paralisi periodica familiare/Miatonia periodica/Sindrome di Cavare'-Romberg-Westfal/Neurosi di Westfal/Paralisi familiare parossistica/Paralisi spinale intermittente/Mioplegia familiare/Miatonia periodica/Mioplegia intermittente]••
Westphall, maladie de[Paralysie périodique type 1, hypokaliémique]
••{
154000
}
*
Weyers acrofacciale disostosi
••••{}
* Whelan Sindrome di•
Whelan syndrome
••{}
*
WHIPPLE MALATTIA DI
/
Whipple Malattia di
[Morbo di Whipple/Lipodistrofia intestinale/Steatorrea idiopatica/Lipogranulomatosi intestinale/Lipofagia granulomatosa/Sprue non tropicale]•
Whipple's Disease
•
Whipple, maladie de[Lipodystrophie intestinale]
••{}
Whitaker Sindrome di
••
Whitaker syndrome de[Apeced syndrome/Hypoadrenocorticisme hypoparathyroidisme moniliase]
••{
240300
}
* White Darier Malattia di•••
White Darier, Enfermedad de[Disqueratosis Folicular Vegetante/Queratosis Folicular/Psorospermosis Folicular/Darier, Enfermedad de]
•{
124200
}
* White Spot Malattia di•••
White Spot, Enfermedad de[ Von Zambusch, Enfermedad de/Liquen de Wilson/Zambusch, Enfermedad de/Morphea Guttata, Tipo Plano/Liquen Ruber Plano/Liquen Plano Atrófico Escleroso/Liquen Plano]
•{}
*
White Murphy Sindrome di
••
White murphy syndrome de
••{
311280
}
*
Wieacker-Wolff Sindrome di
[WWS/Wieacker Sindrome di]•
Wieacker-Wolff syndrome[WWS/Wieacker-Wolff syndrome/apraxia-oculomotor contractures-muscle atrophy syndrome/contractures-muscle atrophy-oculomotor apraxia syndrome/muscle atrophy-contractures-oculomotor apraxia syndrome]
•
Wieacker-Wolff, syndrome de[(Contractures du pied-atrophie musculaire-apraxie oculomotrice)]
•{
314580
}
*
Wiedemann-Beckwith Sindrome di
[Whiedemann-Beckwith-Combs Sindrome di/Sindrome EMG/Onfalocele, macroglossia e viscero-megalia]•
Wiedemann-Beckwith syndrome[BW/ BWS/Beckwith syndrome/Wiedemann syndrome/Wiedemann-Beckwith syndrome/WBS/Wiedemann-Beckwith-Combs syndrome/Exomphalos-macroglossia-gigantism syndrome /EMG syndrome/Familial macroglossia-omphalocele syndrome/Macroglossia-omphalocele syndrome/Macroglossia-omphalocele-visceromegaly syndrome]
•
Wiedemann-Beckwith, syndrome de
•
Wiedmann Beckwith, Síndrome de
••{
130650
}
* Wiedemann tipo 2 Sindrome di[Sindrome Proteus]•
Wiedemann syndrome 2[proteiform syndrome/Proteus syndrome/PS]
••{
176920
}
* Wiedemann-Rautenstrauch (WR) Sindrome di[Sindrome progeroide congenita pseudoidrocefalica]•
Wiedemann Rautenstrauch Syndrome
/
Wiedemann-Rautenstrauch (WR) syndrome[Congenital pseudohydrocephalic progeroid syndrome/Neonatal progeroid syndrome/Neonatal pseudohydrocephalic progeroid syndrome]
•
Wiedemann rautenstrauch syndrome de
••{
264090
}
*
Wiedemann Grosse Dibbern Sindrome di
••
Wiedemann grosse dibbern syndrome de
••{}
*
Wiedemann Oldigs Oppermann Sindrome di
••
Wiedemann oldigs oppermann syndrome de
••{}
*
Wiedemann Opitz Sindrome di
••
Wiedemann opitz syndrome de
••{}
*
Wiedemann Tautenstrauch Sindrome di
••••{}
*
WILDERVANCK SINDROME DI
/
Wildervanck Sindrome di
[Sindrome cervico-oculo-acustica/Anomalia di Klippe-Feil plus]•
Wildervanck Syndrome
•
Wildervanck syndrome de
••{}•(
RN1260
)•
M
* Wildervanck-Smith Sindrome di[Disostosi Acrofacciale Postassiale/POADS/Sindrome di Miller/Sindrome di Genée Wildervanck]•
Wildervanck-Smith syndrome[Genée-Wiedemann acrofacial dysostosis/GWAFD/Genée-Wiedemann syndrome/Miller syndrome/Postaxial acrofacial dysostosis syndrome/POADS]
•••{
263750
}
*
Wilkes Stevenson Sindrome di
••
Wilkes stevenson syndrome de
••{}
*
Wilkie Taylor Scambler Sindrome di
••
Wilkie taylor scambler syndrome de[Cataracte microphtalmie cardiopathie]
••{
601364
}
*
Willebrand Malattia di
[Pseudoemofilia/Angioemofilia/ Sindrome di Willebrand-Jurgens/ Sindrome di Minotvon Willebrand/Trombopatia costituzionale/Tromboastenia emorragica ereditaria/Emofilia vascolare]•
Von Willebrand disease[VWD/Von Willebrand factor, deficiency of/(Von Willebrand factor/factorR VIII-Von Willebrand factor/F8VWF)]
•
Willebrand, maladie de[(Willebrand, forme acquise, maladie de/Willebrand, forme dominante, maladie de/Willebrand, forme récessive, maladie de)]
••{
277480
}
* Willebrand Juergens Malattia di•••
Willebrand Juergens, Enfermedad [Von Willebrand, Enfermedad de/Hemofilia Vascular/Pseudohemofilia/Minot Von Willebrand, Enfermedad de/Trombopatía Constitucional/Angiohemofilia]
•{
193400
-
277480
-
314560
}
*
Willems de Vries Sindrome di
••
Willems de vries syndrome de
••{}
*
Willi-Prader Sindrome di
[Sindrome di Prader Willi]•
Prader- Willi Syndrome[PWS/Prader-Labhart-Willi Syndrome]
•
Willi-Prader, syndrome de[Prader-Willi, syndrome de]
••{
176270
}
*
WILLIAMS SINDROME DI
/
Williams Sindrome di
[Sindrome diWilliams-Beuren/Sindrome di Williams-Barratt/Ipercalcemia idiopatica]•
Williams Syndrome
/
Williams syndrome[WMS/WS/Beuren syndrome/Fanconi-Schlesinger syndrome/Williams-Barratt syndrome/Williams-Beuren syndrome/WBS/elfin facies syndrome/elfin-facies hypercalcemia syndrome/hypercalcemia-peculiar facies-supravalvular aortic stenosis syndrome/hypercalcemia/Williams-Beuren syndrome/idiopathic hypercalcemia-supravalvular aortic stenosis syndrome/mental retardation-typical facies-aortic stenosis syndrome]
•
Williams, syndrome de
•
Williams, Síndrome de
•{
194050
}•
D
•
S
*
WILMS TUMORE DI
[Sindrome di Wilms/Tumore embrionario del rene/Nefroblastoma /Embrioma del rene/Tumore misto del rene]/
Wilms tumore di, aplasia radiale bilaterale
•
Wilms' Tumor
/
Wilms tumor-aniridia syndrome
/
Wilms tumor-aniridia-genitourinary abnormalities-mental retardation triad
/
Wilms tumor-aniridia-gonadoblastoma-mental retardation (WAGR) syndrome, association
•
Wilms tumeur aplasie radiale bilaterale
••{
194070
}•
D
*
WILSON, MALATTIA DI
/
MALATTIA DI WILSON/Morbo di Wilson
/
Wilson, malattia di
[Degenerazione epatolenticolare/Degenerazione neuropatica/Malattia di Kinnier-Wilson/Sindrome di Westphal-Strumpell]•
Wilson's Disease
•
Wilson, maladie de
•
Wilson, Enfermedad de
•{
277900
}•
D
*
Wilson Turner Sindrome di
•
Wilson-Turner syndrome [WTS
/
Wilson-Turner X-linked mental retardation syndrome/Mental retardation, X-linked, syndromic 6/MRXS6/Mental retardation, X-linked, with gynecomastia and obesity]
•
Wilson turner syndrome de[Retard mental gynecomastie obesite lie a l x]
••{
309585
}
*
WINCHESTER SINDROME DI
/
Winchester Malattia di
•
Winchester Syndrome
•
Winchester maladie de
••{
277950
}
*
Winkelman Bethge Pfeiffer Sindrome di
•
Deafness, sensorineural, with dwarfism
•
Winkelman bethge pfeiffer syndrome de[Surdite nanisme pituitaire]
••{
221750
}
*
Winship Viljoen Leary Sindrome di
••
Winship viljoen leary syndrome de[Microcephalie cardiomyopathie]
••{
251220
}
Winter Harding Hyde Sindrome di
••
Winter harding hyde syndrome de[Pachygyrie raideur articulaire anomalies faciales]
••{}
*
Winter Shortland Temple Sindrome di
[Idrocefalo anomalie scheletriche bassa statura]••
Winter shortland temple syndrome de[Hydrocephalie squelette anomalies petite taille]
••{}
*
Wisconsin Sindrome di
•
Wisconsin syndrome
•
Wisconsin syndrome de
••{}
*
Wiskott-Aldrich Sindrome di
[Trombocitopenia, eczema e ripetute infezioni/Sindrome di Aldrich/Sindrome di Aldrich-Dees/Sindrome di Wiskott-Aldrich-Huntley]•
Wiskott Aldrich Syndrome
•
Wiskott-Aldrich, syndrome de
•
Wiskott Aldrich, Síndrome de
[Inmunodeficiencia Tipo Wiskott Aldrich/Aldrich, Síndrome de/Eczema, Trombocitopenia e Inmunodeficiencia]•{
301000
}
*
Wissler-Fanconi Sindrome di
[Subsepsi iperergica /Subsepsis allergica/Sindrome pseudosetticemica/Sindrome di Wissler]••
Wissler-Fanconi, syndrome de
• •{}
*
Witkop Sindrome di
[Ipodonzia disgenesia ungueale]•Witkop Syndrome[Dysplasia of Nails with Hypodontia Tooth-and-Nail Syndrome]•
Witkop syndrome de
••{
189500
}
* Wittmaack Ekbom Sindrome di• Acromelalgia, Hereditay[Restless Legs Syndrome/RLS]••
Wittmaack Ekbom, Síndrome de[Anxietas Tibialis/Acromelalgia Hereditaria/Acromelalgia/Piernas Inquietas, Síndrome de las/Ekbom, Síndrome de]
•{
102300
}
* Wittwer Sindrome di•
Wittwer syndrome
•••{}
*
WL Sindrome
[Sinfalangismo brachidattilia/Stenosi multiple brachidattilia]•WL Syndrome[Multiple Synostoses Syndrome 1/ SYNS1/Synostoses, Multiple, with Brachydactyly/Symphalangism-Brachydactyly Syndrome/Deafness-Symphalangism Syndrome of Herrmann/Facioaudiosymphalangism Syndrome]•
Wl syndrome
••{
186500
}
* Wohlfart Kugelberg Welander Malattia di[Amiotrofia spinale progresiva pura prossimale infantile/Atrofia muscolare giovanile eredofamiliare/Atrophia musculorum pseudo myopathica/Sindrome di Wohlfart-Kugelberg-Welander]•••
Wohlfart Kugelberg Welander, Enfermedad de
•{}
*
Wolcott Rallison Sindrome di
/
Wolcott-Rallison Sindrome di
•
Wolcott-Rallison syndrome
•
Wolcott-Rallison, syndrome de[Dysplasie épiphysaire multiple, diabète précoce]
••{
226980
}
* Wolf Sindrome di•
Wolf syndrome[Chromosome 4p deletion syndrome/Wolf-Hirschhorn syndrome (WHS/4p- syndrome/4p deletion syndrome/chromosome 4p monosomy/del(4p) syndrome/monosomy 4p/partial monosomy 4p]
•••{
194190
}
*
WOLF-HIRSCHHORN SINDROME DI
/
Wolf-Hirschhorn Sindrome di
•
Wolf Hirschhorn Syndrome
/
Wolf-Hirschhorn syndrome (WHS)
•
Wolf-Hirschhorn, syndrome de
••{
194190
}•
D
•
S
•
A
*
Wolff Parkinson White Sindrome di
/
Wolff-Parkinson-White Sindrome di
[Eccitazione atrio-ventricolare anomala/Sindrome da preeccitazione/Falso blocco di branca]•
Wolff Parkinson White Syndrome
[Auriculoventricular accessory pathway syndrome]•
Wolff-Parkinson-White, syndrome de
[WPW Syndroma/(Preexcitation syndrome/Accessory atrioventricular pathways)]•
Wolff Parkinson White, Síndrome de[WPW, Síndrome de/Preexcitación, Síndrome de/Vías Atrioventriculares Accesorias]
•{
194200
}
*
Wolff Zimmermann Sindrome di
•
Wolff mental retardation syndrome
•
Wolff zimmermann syndrome de[Retard mental type wolff]
••{
277990
}
*
WOLFRAM SINDROME DI
/
Wolfram Sindrome di
[Diabete mellito e atrofia ottica semplice in gemelli]•
Wolfram Syndrome
/
Wolfram syndrome
•
Wolfram, syndrome de
•
Wolfram, Síndrome de
•{
222300
-
598500
}
*
Wolman Malattia di
[Xantomatosi primaria familiare con calcificazione surrenalica/Xantomatosi generalizzata con surrenali calcificate/Tesaurismosi degli esteri del colesterolo/Xantomatosi di Wolman]•
Wolman disease[Lysosomal acid lipase deficiency/LIPA deficiency/LAL deficiency/Acid cholesteryl ester hydrolase deficiency, Wolman Type/Cholesterol ester hydrolase deficiency/Cholesterol ester storage disease/ CESD/Cholesteryl ester storage disease/Acid Cholesteryl ester hydrolase deficiency, Type 2/(Lipase A, Lysosomal acid/LIPA/Cholesterol ester hydrolase)]
•
Wolman, maladie de[Esters du cholestérol, maladie de stockage en/Lipase acide lysosomale, déficit en]
••{
278000
}
*
Woodhouse Sakati Sindrome di
••
Woodhouse sakati syndrome de[Diagete hypogonadisme surdite retard mental]
••{
241080
}
* Woods Sindrome di•
Woods syndrome
[Syndactyly, Type I, with Microcephaly and Mental Retardation/Filippi Syndrome]•••{
272440
}
*
Woods Black Norbury Sindrome di
••
Woods black norbury syndrome de[Mort neonatale deficit immunitaire]
••{
600486
}
*
Woods Leversha Rogers Sindrome di
••
Woods leversha rogers syndrome de[Retard de croissance sensibilite a la mitomycine]
••{}
*
Worster Drought Sindrome di
•
Worster-Drought syndrome[congenital suprabulbar paresis]
•
Worster drought syndrome[Paresie suprabulbaire congenitale]
••{
185480
}
*
Worth Sindrome di
••
Worth syndrome de[Osteosclerose type worth autosomique dominante/Hyperostose endosteale type worth]
••{
144750
}
*
Wright Dyck Sindrome di
[Neuropatia sensoriale sordità demenza]••
Wright dyck syndrome de[Neuropathie sensorielle surdite demence]
••{}
*
WT arti sangue Sindrome
•WT Limb-Blood Syndrome•••{
194350
}
* Wyburn Mason Sindrome di[Aneurisma arterovenoso cerebro-retinico/Aneurisma arterovenoso della retina e dell'encefalo]•
Wyburn Mason Syndrome
••
Wyburg Mason, Síndrome de [Aneurisma Arteriovenoso Cerebroretinal, Síndrome del]
•{}
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