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W Syndrome
Waaler Aarskog Syndrome (Hydrocephalus with Costovertebral Dysplasia and Sprengel Anomaly)
Waardenburg Syndrome
List of Sites
-(Recessive) Anophthalmia Syndrome
-Shah Syndrome
with Hirschsprung Disease
Wagner Syndrome (Erosive Vitreoretinopathy, Hyaloideoretinal Degeneration of Wagner, Wagner Vitreoretinal Degeneration)
Wagner-Stickler Syndrome
WAGR Syndrome
Walbaum Titran Durieux Crepin Syndrome (Fibular Hypoplasia with Scapulo Pelvic Dysplasia and Absent 5th Fingers)
Walker Dyson Syndrome (Aniridia-Mental Retardation Syndrome)
Walker Warburg Syndrome (Cerebroocular Dysgenesis; Cerebroocular Dysplasia-Muscular Dystrophy Syndrome; Chemke Syndrome; COD-MD Syndrome; Hard +/- E Syndrome; H ydrocephalus, A gyria, and R etinal D ysplasia [HARD ] Syndrome; Pagon Syndrome)
Wallis Cremin Beighton Syndrome (Enchondromatosis with Dwarfism and Deafness)
Wallis Zieff Goldblatt Syndrome (Cleidorhizomelic Syndrome)
Walt Disney Dwarfism (Geroderma Osteodysplastica)
Warburg (Micro/Sjo Fledelius) Syndrome
Warburton Anyane Yeboa Syndrome (Mosaic Variegated Aneuplody Microcephaly Syndrome)
Warfarin Antenatal Infection
Warman Mulliken Hayward Syndrome (Craniosynostosis, Warman Type)
Warman Mulliken Syndrome (Craniosynostosis, Autosomal Dominant)
Watson Miller Syndrome
Watson Syndrome (Café-au-Lait Spots with Pulmonic Stenosis)
Weaver Syndrome (Camptodactyly with Overgrowth and Unusual Facies)
Weaver-Like Syndrome
Weaver Johnson Syndrome (Craniosynostosis Cleft Lip Palate Arthrogryposis)
Weaver Williams Syndrome
Wegmann Jones Smith Syndrome (Short Limb Dwarfism with Oedema and Iris Coloboma)
Wiedemann's Syndrome
Weill Marchesani Syndrome (Mesodermal Dysmorphodystrophy, Congenital; Spherophakia Brachymorphia Syndrome)
Weinstein Kliman Scully Syndrome (Cardiomyopathy with Hypogonadism and Metabolic Anomalies)
Weismann Netter (Stuhl) Syndrome (Anterior Bowing of the Legs with Dwarfism; Skeletal Dysplasia, Weismann Netter Stuhl Type; Toxopachyosteose [Diaphysaire Tibio-Peroniere])
Weissenbacher Zweymuller Syndrome (Pierre Robin Syndrome with Fetal Chondrodysplasia)
Welander Distal Myopathy
Weleber Hecht Bigley Syndrome (Cataract with Hyperostosis Frontalis and Dislocating Patella)
Wellesley Carmen French Syndrome (Cataract Aberrant Oral Frenula Growth Retardation)
Werdnig Hoffmann Disease
Wermer Syndrome (Endocrine Neoplasia, Multiple, Type I; Endocrine Adenomatosis, Multiple)
Werner Syndrome
Wernicke Korsakoff Syndrome (Transketolase Defect; Alcohol-Induced Encephalopathy)
West Syndrome(, X-Linked) (Infantile Spasm Syndrome)
Westerhof Beemer Cormane Syndrome (Macules, Hereditary Congenital Hypopigmented and Hyperpigmented)
Westphall Disease (Periodic Paralysis, Type 1/Hypokaliemic)
Weyers' Syndrome (Weyers Acrofacial Dysostosis)
Whistling Face-Windmill Vane Hand Syndrome
Whitaker Syndrome (APECED Syndrome; Autoimmune Polyendocrinopathy Syndrome, Type I; Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy; Autoimmune Polyglandular Syndrome, Type I; Hypoadrenocorticism Hypoparathyroidism Moniliasis; Polyglandular Autoimmune Syndrome, Type I)
White Forelock/Poliosis
Whyte Syndrome (Spondyloepimetaphyseal Dysplasia with Hypotrichosis)
Whyte Murphy Syndrome (Osteopathia Striata with Pigmentary Dermopathy and White Forelock)
Wieacker (Wolff) Syndrome (Contractures of Feet-Muscle Atrophy-Oculomotor Apraxia, WWS)
Wiedemann Grosse Dibbern Syndrome (Microcephaly with Micropenis and Convulsions)
No Information Available Online
Wiedemann Oldigs Oppermann Syndrome (Hirsutism-Skeletal Dysplasia-Mental Retardation Syndrome)
Wiedemann Opitz Syndrome (Polydactyly with Tibial Defect and Trigonomacrocephaly)
Wiedemann Rautenstrauch Syndrome (Progeroid Syndrome, Neonatal)
Wildervanck Syndrome
Wilkes Stevenson Syndrome
Wilkie Taylor Scambler Syndrome (Cataract with Microphthalmia and Septal Defect)
Willebrand Disease
Willems de Vries Syndrome (Short Limbs with Subluxed Knees and Cleft Palate)
William('s) (Beuren) Syndrome
Wilms Tumor (Nephroblastoma)
List of Sites
with Pseudohermaphroditism
-Aniridia Syndrome
-Aniridia-Genitourinary Anomalies-Mental Retardation (WAGR) Syndrome/Triad
with Radial Bilateral Aplasia
Wilson('s) Disease (Hepatolenticular Degeneration)
Wilson Turner (X-Linked Mental Retardation) Syndrome (Mental Retardation, X-Linked, Syndromic 6; Mental Retardation, X-Linked, with Gynecomastia and Obesity)
Winchester (Grossman) Disease/Syndrome
Winkelman Bethge Pfeiffer Syndrome (Deafness, Neurosensory, with Pituitary Dwarfism)
Winship Ocular Albinism
Winship Viljoen Leary Syndrome (Microcephaly-Cardiomyopathy)
Winter Harding Hyde Syndrome (Pachygyria with Joint Contractures and Facial Abnormalities)
Winter Shortland Temple Syndrome (Hydrocephalus with Growth Retardation and Skeletal Anomalies)
Wiskott Aldrich Syndrome (Eczema-Thrombocytopenia-Immunodeficiency Syndrome; Immunodeficiency, Type 2/Wiskott Aldrich Type)
Witkop Ocular Albinism
Witkop Syndrome (Hypodontia with Dysplasia of Nails, Tooth and Nail Syndrome)
WL Syndrome (Deafness-Symphalangism Syndrome of Herrmann; Facioaudiosymphalangism Syndrome; Multiple Synostoses Syndrome, Type I; Symphalangism-Brachydactyly Syndrome; Synostoses, Multiple, with Brachydactyly)
Wolcott Rallison Syndrome (Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus; IDDM-MED Syndrome)
Wolf (Hirschhorn) Syndrome (Deletion/Monosomy 4p, WHS)
Wolff Mental Retardation Syndrome
Wolff Parkinson White Syndrome
Wolff Zimmermann Syndrome (Mental Retardation, Wolff Type; Wolff Mental Retardation Syndrome)
Wolfram Syndrome (D iabetes I nsipidus, D iabetes M ellitus, O ptic A trophy, and D eafness [DIDMOAD ] Syndrome)
Wolman('s) Disease (Cholesterol Ester Storage Disease, Lysosomal Acid Lipase Deficiency)
Woodhouse Sakati Syndrome (Diabetes Mellitus with Hypogonadism, Alopecia, Deafness, Electrocardiographic Abnormalities and Mental Retardation)
Woods Black Norbury Syndrome (Immunoneurologic Disorder, X-Linked; Neonatal with Death Immune Deficiency)
Woods Leversha Rogers Syndrome (Microcephaly with Developmental Delay and Pancytopenia)
Wooly/Woolly Hair
Autosomal Dominant
Congenital (Woolly Hair Syndrome)
Syndrome
with Hypotrichosis, Everted Lower Lip and Outstanding Ears
with Palmoplantar Keratoderma and Cardiac Anomaly
See Naxos Disease
Worster Drought Syndrome (Suprabulbar Paresis, Congenital)
Worth Syndrome (Endosteal Hyperostosis, Worth Type; Osteosclerosis, Autosomal Dominant, Worth Type)
Wright Dick Syndrome (Sensory Neuropathy with Deafness and Dementia)
Wrinkly Skin Syndrome
WT Limb-Blood Syndrome
Wyburn-Mason Syndrome (Bonnet-Dechaume-Blanc Syndrome)
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