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W Syndrome Waaler Aarskog Syndrome (Hydrocephalus with Costovertebral Dysplasia and Sprengel Anomaly) Waardenburg Syndrome 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; Hydrocephalus, Agyria, and Retinal Dysplasia [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)
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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) 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 (Diabetes Insipidus, Diabetes Mellitus, Optic Atrophy, and Deafness [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 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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