Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program W/1 ENGLISH

Browse A-Z | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program







W/1



Browse the GARD list of rare diseases and related terms to find topics of interest to you. This list includes the main name for each condition, as well as alternate names. Inclusion on this list does not serve as official recognition by the NIH that a disease is rare. Some conditions that are not considered rare are on this list and are labeled accordingly.Read more about which diseases are included on the GARD website.

• W syndrome - See Pallister W syndrome
• Waaler-Aarskog syndrome - See Hydrocephalus, costovertebral dysplasia, and Sprengel anomaly
• Waardenburg anophthalmia syndrome - See Anophthalmos with limb anomalies
• Waardenburg syndrome
• Waardenburg syndrome type 1
• Waardenburg syndrome type 2
• Waardenburg syndrome type 2A
• Waardenburg syndrome type 2B
• Waardenburg syndrome type 3
• Waardenburg syndrome type 4
• Waardenburg syndrome with upper limb anomalies - See Waardenburg syndrome type 3
• Waardenburg syndrome, type 3 - See Waardenburg syndrome type 3
• Waardenburg-Hirschsprung disease - See Waardenburg syndrome type 4
• Waardenburg-Hirschsprung syndrome - See Waardenburg syndrome type 4
• Waardenburg's syndrome type 1 - See Waardenburg syndrome type 1
• Waardenburg-Shah syndrome - See Waardenburg syndrome type 4
• Wadia Swami syndrome - See Spinocerebellar ataxia 2
• Wagenmann-froboese syndrome - See Multiple endocrine neoplasia type 2B
• Wagner disease (formerly) - See Wagner syndrome
• Wagner syndrome
• Wagner syndrome type 1 - See Wagner syndrome
• Wagner vitreoretinal degeneration - See Wagner syndrome
• WAGR Complex - See WAGR syndrome
• WAGR syndrome
• Waisman syndrome - See Early-onset parkinsonism-intellectual disability syndrome
• Walbaum Titran Durieux Crepin syndrome
• Waldenstrom macroglobulinemia
• Waldenstrom's macroglobulinaemia - See Waldenstrom macroglobulinemia
• Waldenstrom's syndrome - See Waldenstrom macroglobulinemia
• Waldmann disease - See Primary intestinal lymphangiectasia
• Waldmann's disease - See Primary intestinal lymphangiectasia
• Walker Dyson syndrome
• Walker-Clodius syndrome - See EEC syndrome
• Walker-Warburg syndrome
• Wallenberg syndrome
• Wallenberg's syndrome - See Wallenberg syndrome
• Wallerian degeneration
• Wallerian degeneration of the pyramidal tract - See Wallerian degeneration
• Wallet sciatica - See Piriformis syndrome
• Wallis cremin beighton syndrome - See Enchondromatosis dwarfism deafness
• Wallis Zieff Goldblatt syndrome - See Cleidorhizomelic syndrome
• Walt Disney dwarfism - See Geroderma osteodysplastica
• Wandering spleen
• WARBM - See Micro syndrome
• Warburg micro syndrome - See Micro syndrome
• Warburg syndrome - See Walker-Warburg syndrome
• Warburg Thomsen syndrome - See Yemenite deaf-blind hypopigmentation syndrome
• Warburton-Anyane-Yeboa syndrome - See Mosaic variegated aneuploidy syndrome
• Ward-Romano syndrome - See Long QT syndrome 1
• Warfarin embryofetopathy - See Warfarin syndrome
• Warfarin embryopathy - See Warfarin syndrome
• Warfarin resistance
• Warfarin sensitivity
• Warfarin syndrome
• Warm antibody AIHA - See Warm antibody hemolytic anemia
• Warm antibody autoimmune hemolytic anemia - See Warm antibody hemolytic anemia
• Warm antibody hemolytic anemia
• Warman Mulliken Hayward syndrome
• Warm-reacting-antibody hemolytic anemia - See Warm antibody hemolytic anemia
• Warsaw breakage syndrome
• Warthin tumor
• Warts in the throat - See Laryngeal papillomatosis
• Warts, Hypogammaglobulinemia, Infections, and Myelokathexis - See WHIM syndrome
• WAS - See Wiskott Aldrich syndrome
• WAT - See Wolffian tumor
• Waterhouse-Friderichsen syndrome - See Waterhouse–Friderichsen syndrome
• Waterhouse–Friderichsen syndrome
• Watermelon stomach
• Watery Diarrhea Syndrome - See WDHA syndrome
• Watery diarrhea, hypokalemia, and achlorhydria syndrome - See WDHA syndrome
• Watson Alagille syndrome - See Alagille syndrome
• Watson syndrome
• Watson-Miller syndrome - See Alagille syndrome
• WBP syndrome - See Winkelman Bethge Pfeiffer syndrome
• WBS - See Williams syndrome
• WBS duplication syndrome - See 7q11.23 duplication syndrome
• WD - See Wilson disease
• WDHA syndrome
• WDM - See Welander distal myopathy, Swedish type
• WDSTS - See Wiedemann-Steiner syndrome
• Weaver Johnson syndrome
• Weaver like syndrome - See Weaver syndrome
• Weaver Smith syndrome - See Weaver syndrome
• Weaver syndrome
• Weaver Williams syndrome
• Weber Christian disease - See Nodular nonsuppurative panniculitis
• Weber syndrome
• Weber-Christian disease - See Nodular nonsuppurative panniculitis
• Weber-Cockayne syndrome - See Epidermolysis bullosa simplex, localized
• Weber-Cockayne type epidermolysis bullosa simplex - See Epidermolysis bullosa simplex, localized
• Weber-Klippel-Trenaunay - See Klippel-Trenaunay syndrome
• Wedge-shaped epiphyses of knees - See Metaphyseal acroscyphodysplasia
• Wedge-shaped epiphyses of the knees with mental retardation and short stature - See Metaphyseal acroscyphodysplasia
• WEE - See Western equine encephalitis
• Wegener granulomatosis - See Granulomatosis with polyangiitis
• Wegmann Jones Smith syndrome
• Weight loss, necrolytic migratory erythema (NME), diabetes, stomatitis, and diarrhea - See Glucagonoma syndrome
• Weil Disease - See Leptospirosis
• Weill-Marchesani syndrome
• Weinstein Kliman Scully syndrome
• Weismann Netter syndrome - See Bowing of legs, anterior with dwarfism
• Weissenbacher-Zweymuller syndrome
• Weissenbacher-Zweymüller syndrome - See Weissenbacher-Zweymuller syndrome
• Welander distal myopathy - See Welander distal myopathy, Swedish type
• Welander distal myopathy, Swedish type
• Weleber Hecht Bigley syndrome
• Well-differentiated NEN of pancreas - See Pancreatic neuroendocrine tumor
• Well-differentiated neuroendocrine neoplasm of pancreas - See Pancreatic neuroendocrine tumor
• Well-differentiated pancreatic NEN - See Pancreatic neuroendocrine tumor
• Well-differentiated pancreatic neuroendocrine neoplasm - See Pancreatic neuroendocrine tumor
• Wellesley Carmen French syndrome
• Wells syndrome
• Wells' syndrome - See Wells syndrome
• Wells-Jankovic syndrome
• Werdnig Hoffmann disease - See Spinal muscular atrophy 1
• Werdnig-Hoffmann disease - See Spinal muscular atrophy 1
• Wermer syndrome - See Multiple endocrine neoplasia type 1
• Werner syndrome - See Werner's syndrome
• Werner-like syndrome due to combined growth factor deficiency - Another name for Lipodystrophy due to peptidic growth factors deficiency
• Werner's syndrome
• Wernicke-Korsakoff syndrome
• West nile encephalitis
• West nile virus
• West syndrome
• Westerhof Beemer Cormane syndrome - See Macules hereditary congenital hypopigmented and hyperpigmented
• Western equine encephalitis
• Western equine encephalomyelitis - See Western equine encephalitis
• West's syndrome - See West syndrome
• Weyers acrofacial dysostosis
• Weyers ulnar ray/oligodactyly syndrome
• WFS - See Wolfram syndrome
• WG - See Granulomatosis with polyangiitis
• WGN1 - See Wagner syndrome
• WHH syndrome - See Winter Harding Hyde syndrome
• WHIM syndrome
• WHIMS - See WHIM syndrome
• Whipple disease
• Whipworm infection - See Trichuriasis
• Whispering dysphonia - See DYT-TUBB4A
• Whistling face syndrome, recessive form
• Whistling face-windmill vane hand syndrome - See Freeman Sheldon syndrome
• Whitaker syndrome - See Autoimmune polyglandular syndrome type 1
• White forelock (poliosis) syndrome with multiple congenital malformations - See Waardenburg syndrome type 3
• White forelock and leukoderma with neurological impairment - See Telfer Sugar Jaeger syndrome
• White forelock with malformations
• White liver disease - See Visceral steatosis
• White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome
• White platelet syndrome
• White sponge nevus of cannon
• Whitmore disease - See Melioidosis
• WHO Grade II Ependymal Neoplasm - See Ependymoma
• Whooping cough
• WHS - See Wolf-Hirschhorn syndrome
• Whyte Murphy syndrome - See Osteopathia striata with pigmentary dermopathy including white forelock
• Whyte Petersen McAlister syndrome - See Spondyloepimetaphyseal dysplasia with hypotrichosis
• Whyte syndrome - See Spondyloepimetaphyseal dysplasia with hypotrichosis
• Widened medullary cavities of bone, aortic calcification, abnormal dentition, and muscular weakness - See Singleton-Merten syndrome
• Wieacker syndrome - See Intellectual disability-developmental delay-contractures syndrome
• Wieacker Wolff syndrome - See Intellectual disability-developmental delay-contractures syndrome
• Wiedemann Grosse Dibbern syndrome - See Wiedemann-Steiner syndrome
• Wiedemann Oldigs Oppermann syndrome
• Wiedemann Opitz syndrome
• Wiedemann Rautenstrauch syndrome - See Neonatal progeroid syndrome
• Wiedemann-Beckwith Syndrome (WBS) - See Beckwith-Wiedemann syndrome
• Wiedemann-Oldigs-Oppermann syndrome - See Wiedemann Oldigs Oppermann syndrome
• Wiedemann-Rautenstrauch syndrome - See Neonatal progeroid syndrome
• Wiedemann-Steiner syndrome
• Wildervanck syndrome
• Wildervanck-Smith syndrome - See Miller syndrome
• Wilkes Stevenson syndrome
• Wilkie syndrome - See Superior mesenteric artery syndrome
• Willebrand disease, acquired - See Acquired Von Willebrand syndrome
• Willems De vries syndrome
• Williams syndrome
• Williams-Beuren region duplication syndrome - See 7q11.23 duplication syndrome
• Williams-Beuren syndrome - See Williams syndrome
• Willi-Prader syndrome - See Prader-Willi syndrome
• Willis Ekbom disease - See Restless legs syndrome - not a rare disease
• Wilms' tumor
• Wilms tumor 5 - See Wilms tumor and radial bilateral aplasia
• Wilms tumor and pseudohermaphroditism - See Denys-Drash syndrome
• Wilms tumor and radial bilateral aplasia
• Wilms tumor, Aniridia, Genitourinary anomalies, mental Retardation syndrome - See WAGR syndrome
• Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome - See WAGR syndrome
• Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation syndrome - See WAGR syndrome
• Wilson disease
• Wilson Turner mental retardation syndrome (formerly) - See Wilson-Turner syndrome
• Wilson-Mikity syndrome
• Wilson-Turner syndrome
• Winchester syndrome - See Torg Winchester syndrome
• Winchester-Grossman syndrome - See Torg Winchester syndrome
• Windblown hand
• Windswept hand - See Windblown hand
• Winged helix deficiency - See T-cell immunodeficiency, congenital alopecia and nail dystrophy
• Winkelman Bethge Pfeiffer syndrome
• Winkelmann-Bethge-Pfeiffer syndrome - See Pituitary hormone deficiency, combined 3
• Winship-Viljoen-Leary syndrome - See Microcephaly-cardiomyopathy
• Winter Harding Hyde syndrome
• Wisconsin syndrome
• Wiskott Aldrich syndrome
• Witkop syndrome
• Wittwer syndrome - See Wolf-Hirschhorn syndrome
• WL syndrome - See Multiple synostoses syndrome 1
• WM Syndrome - See Weill-Marchesani syndrome
• WMS - See Weill-Marchesani syndrome
• WMS - See Williams syndrome
• WND - See Wilson disease
• WNS - See Bowing of legs, anterior with dwarfism
• Wolcott Rallison syndrome - See Epiphyseal dysplasia multiple with early-onset diabetes mellitus
• Wolf syndrome - See Wolf-Hirschhorn syndrome
• Wolffian adenoma - See Wolffian tumor
• Wolffian adnexal tumor - See Wolffian tumor
• Wolffian tumor
• Wolff-Parkinson-White syndrome - not a rare disease
• Wolf-Hirschhorn syndrome
• Wolfram syndrome
• Wolman disease
• Woodhouse Sakati syndrome
• Woodhouse-Sakati syndrome - See Woodhouse Sakati syndrome
• Woods Black Norbury syndrome
• Woods syndrome - See Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome
• Woods-Crouchman-Huson syndrome - See Microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome
• Wool sorter's disease - See Anthrax
• Woolly hair - See Woolly hair syndrome
• Woolly hair hypotrichosis everted lower lip and outstanding ears
• Woolly hair palmoplantar keratoderma cardiac abnormalities - See Naxos disease
• Woolly hair syndrome
• Woolly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome - See Cardiomyopathy dilated with woolly hair and keratoderma
• Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome - See Cardiomyopathy dilated with woolly hair and keratoderma
• Wooly hair - palmoplantar keratoderma - dilated cardiomyopathy - See Cardiomyopathy dilated with woolly hair and keratoderma
• Wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome - See Cardiomyopathy dilated with woolly hair and keratoderma
• Wooly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome - See Cardiomyopathy dilated with woolly hair and keratoderma
• Worm infections - See Helminthiasis
• Worster Drought syndrome
• Worth syndrome - See Worth type autosomal dominant osteosclerosis
• Worth type autosomal dominant osteosclerosis
• Wound botulism (subtype) - See Botulism
• WPW syndrome - See Wolff-Parkinson-White syndrome - not a rare disease
• Wrinkly skin syndrome
• WRN - See Werner's syndrome
• WS 2 - See Waardenburg syndrome type 2
• WS type 2 - See Waardenburg syndrome type 2
• WS1 - See Waardenburg syndrome type 1
• WS2A - See Waardenburg syndrome type 2A
• WS2B - See Waardenburg syndrome type 2B
• WS3 - See Waardenburg syndrome type 3
• WS4 - See Waardenburg syndrome type 4
• WSN - See Early-onset parkinsonism-intellectual disability syndrome
• WSN - See White sponge nevus of cannon
• WSS - See Weaver syndrome
• WT limb blood syndrome
• WT1 - See Wilms' tumor
• WT5 - See Wilms tumor and radial bilateral aplasia
• WTS - See Wilson-Turner syndrome
• WTsyndrome - See WT limb blood syndrome
• Wuchereria Bancrofti infection - See Lymphatic filariasis
• Wuchereriasis - See Lymphatic filariasis
• WWS - See Intellectual disability-developmental delay-contractures syndrome
• Wyburn Mason syndrome - See Wyburn-Mason syndrome
• Wyburn-Mason syndrome
• WZS - See Weissenbacher-Zweymuller syndrome