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Rare Disease Database

Search Results for: W

0-9 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

Waardenburg Syndrome

Also known as: WS
Subdivisions: Waardenburg syndrome type IIA (WS2A), Waardenburg syndrome type IIB (WS2B), Waardenburg syndrome type III (WS3), Waardenburg syndrome type II (WS2), Waardenburg syndrome type IV (WS4), Waardenburg syndrome type I (WS1)

WAGR Syndrome/11p Deletion Syndrome

Also known as: chromosome 11p deletion syndrome, WAGR complex
Subdivisions: AGR triad, aniridia-ambiguous genitalia-mental retardation, aniridia-Wilms' tumor association, aniridia-Wilms' tumor-gonadoblastoma, AWTA

Walker Warburg Syndrome

Also known as: muscular dystrophy-dystroglycanopathy [with brain and eye anomalies], type A (MDDGA), cerebroocular dysplasia-muscular dystrophy syndrome (COD-MD syndrome), hydrocephalus, agyria, and retinal dysplasia (HARD syndrome)

Wandering Spleen

Also known as: Displaced Spleen, Drifting Spleen, Floating Spleen, Pelvic Spleen, Splenic Ptosis, Splenoptosis, Systopic Spleen, WS

WAS Related Disorders

Also known as: WAS, Wiskott Aldrich syndrome, X-linked congenital neutropenia, X-linked thrombocytopenia

Weaver Syndrome

Also known as: Overgrowth syndrome, Weaver-Smith Syndrome, WSS

Weil Syndrome

Also known as: Fiedler Disease, Icteric Leptospirosis, Icterohemorrhagic Leptospirosis, Infectious Jaundice, Lancereaux-Mathieu-Weil Spirochetosis, Leptospiral Jaundice, Spirochetal Jaundice, Weil Disease

Weill Marchesani Syndrome

Also known as: congenital mesodermal dysmorphodystrophy, mesodermal dysmorphodystrophy, congenital, spherophakia-brachymorphia syndrome, WMS, WM syndrome

Weismann Netter Stuhl Syndrome

Also known as: anterior bowing of the legs with dwarfism, skeletal dysplasia, Weismann Netter Stuhl type, toxopachyosteose diaphysaire tibio-peroniere, Weismann-Netter syndrome

Werdnig-Hoffmann Disease

Also known as: infantile spinal muscular atrophy, SMA 1, SMA, infantile acute form, spinal muscular atrophy type 1, Werdnig-Hoffman paralysis

Werner Syndrome

Also known as: Werner’s syndrome, progeria of adults, WS

West Nile Encephalitis

Also known as: Eastern equine encephalitis, EEE, Japanese encephalitis, Kunjin fever, Venezuelan encephalitis, Viral encephalitis, WEE, Western equine encephalitis, West Nile Fever, West Nile virus, WNE

West Syndrome

Also known as: epileptic spasms, infantile spasms
Subdivisions: x linked infantile spasms

WHIM Syndrome

Also known as: warts, hypogammaglobulinemia, infections and myelokathexis syndrome

Whipple Disease

Also known as: Intestinal Lipodystrophy, Intestinal Lipophagic Granulomatosis, Malabsorption Syndrome, Secondary Non-tropical Sprue

Wieacker Syndrome

Also known as: Apraxia, Oculomotor, with Congenital Contractures and Muscle Atrophy, Contractures of Feet, Muscle Atrophy, and Oculomotor Apraxia, Wieacker-Wolff Syndrome, WRWF, intellectual disability-developmental delay-contractures syndrome
Subdivisions: No subdivisions found

Wiedemann Rautenstrauch Syndrome

Also known as: neonatal progeroid syndrome, neonatal pseudo-hydrocephalic progeroid syndrome of WRS, Rautenstrauch-Wiedemann syndrome

Williams Syndrome

Also known as: Beuren Syndrome, Early Hypercalcemia Syndrome with Elfin Facies, Elfin Facies with Hypercalcemia, Hypercalcemia-Supravalvar Aortic Stenosis, WBS, Williams-Beuren Syndrome, WMS

Wilson Disease

Also known as: hepatolenticular degeneration, lenticular degeneration, progressive

Winchester Syndrome

Also known as: Winchester-Grossman syndrome, Torg-Winchester syndrome, Winchester disease, MONA (multicentric osteolysis, nodulosis, and arthropathy)

WNT4 Deficiency

Also known as: Biason-Lauber syndrome, Mullerian aplasia and hyperandrogenism, WNT4 Mullerian aplasia, WNT4 syndrome

Wolfram Syndrome

Also known as: diabetes insipidus, diabetes mellitus, optic atrophy and deafness, DIDMOAD

Wolman Disease

Also known as: acid cholesteryl ester hydrolase deficiency, Wolman type, lysosomal acid lipase deficiency, Wolman type, LAL deficiency, Wolman type
Subdivisions: No subdivisions found