Rare Disease Database

Rare Disease Database

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Rare Disease Database GARD Rare Diseases Database
NORD Rare Disease Report
WHIM Syndrome

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

NORD Rare Disease Report
Whipple Disease

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

NORD Rare Disease Report
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

NORD Rare Disease Report
Wiedemann Rautenstrauch Syndrome

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

NORD Rare Disease Report
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

NORD Rare Disease Report
Wilms’ Tumor

Also known as: embryoma kidney nephroblastoma

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NORD Rare Disease Report
Wilson Disease

Also known as: hepatolenticular degeneration lenticular degeneration, progressive

NORD Rare Disease Report
Winchester Syndrome

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

NORD Rare Disease Report
WNT4 Deficiency

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

NORD Rare Disease Report
Wolfram Syndrome

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

NORD Rare Disease Report
Wolman Disease

Also known as: acid cholesteryl ester hydrolase deficiency, Wolman type lysosomal acid lipase deficiency, Wolman type LAL deficiency, Wolman type

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