List of rare diseases-W
NIH genetic and rare disease info
List of rare diseases-W is a rare disease.
Rare and genetic diseases | ||||||
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Rare diseases - List of rare diseases-W
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- W syndrome
- Waaler-Aarskog syndrome
- Waardenburg anophthalmia syndrome
- 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
- Waardenburg syndrome, type 3
- Waardenburg-Hirschsprung disease
- Waardenburg-Hirschsprung syndrome
- Waardenburg's syndrome type 1
- Waardenburg-Shah syndrome
- Wadia Swami syndrome
- Wagenmann-froboese syndrome
- Wagner disease (formerly)
- Wagner syndrome
- Wagner syndrome type 1
- Wagner vitreoretinal degeneration
- WAGR Complex
- WAGR syndrome
- Waisman syndrome
- Walbaum Titran Durieux Crepin syndrome
- Waldenstrom macroglobulinemia
- Waldenstrom's macroglobulinaemia
- Waldenstrom's syndrome
- Waldmann disease
- Waldmann's disease
- Walker Dyson syndrome
- Walker-Clodius syndrome
- Walker-Warburg syndrome
- Wallenberg syndrome
- Wallenberg's syndrome
- Wallerian degeneration
- Wallerian degeneration of the pyramidal tract
- Wallet sciatica
- Wallis cremin beighton syndrome
- Wallis Zieff Goldblatt syndrome
- Walt Disney dwarfism
- Wandering spleen
- WARBM
- Warburg micro syndrome
- Warburg syndrome
- Warburg Thomsen syndrome
- Warburton-Anyane-Yeboa syndrome
- Ward-Romano syndrome
- Warfarin embryofetopathy
- Warfarin embryopathy
- Warfarin resistance
- Warfarin sensitivity
- Warfarin syndrome
- Warm antibody AIHA
- Warm antibody autoimmune hemolytic anemia
- Warm antibody hemolytic anemia
- Warman Mulliken Hayward syndrome
- Warm-reacting-antibody hemolytic anemia
- Warsaw breakage syndrome
- Warthin tumor
- Warts in the throat
- Warts, Hypogammaglobulinemia, Infections, and Myelokathexis
- WAS
- WAT
- Waterhouse-Friderichsen syndrome
- Waterhouse–Friderichsen syndrome
- Watermelon stomach
- Watery Diarrhea Syndrome
- Watery diarrhea, hypokalemia, and achlorhydria syndrome
- Watson Alagille syndrome
- Watson-Miller syndrome
- WBS
- WBS duplication syndrome
- WD
- WDHA syndrome
- WDM
- WDSTS
- Weaver like syndrome
- Weaver Smith syndrome
- Weaver syndrome
- Weaver Williams syndrome
- Weber Christian disease
- Weber syndrome
- Weber-Christian disease
- Weber-Cockayne syndrome
- Weber-Cockayne type epidermolysis bullosa simplex
- Weber-Klippel-Trenaunay
- Wedge-shaped epiphyses of knees
- Wedge-shaped epiphyses of the knees with mental retardation and short stature
- WEE
- Wegener granulomatosis
- Weil Disease
- Weill-Marchesani syndrome
- Weismann Netter syndrome
- Weissenbacher-Zweymuller syndrome
- Weissenbacher-Zweymüller syndrome
- Welander distal myopathy
- Welander distal myopathy, Swedish type
- Well-differentiated NEN of pancreas
- Well-differentiated neuroendocrine neoplasm of pancreas
- Well-differentiated pancreatic NEN
- Well-differentiated pancreatic neuroendocrine neoplasm
- Wellesley Carmen French syndrome
- Wells syndrome
- Wells' syndrome
- Wells-Jankovic syndrome
- Werdnig Hoffmann disease
- Werdnig-Hoffmann disease
- Wermer syndrome
- Werner 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
- Western equine encephalitis
- Western equine encephalomyelitis
- West's syndrome
- Weyers acrofacial dysostosis
- Weyers ulnar ray/oligodactyly syndrome
- WFS
- WG
- WGN1
- WHH syndrome
- WHIM syndrome
- WHIMS
- Whipple disease
- Whipworm infection
- Whispering dysphonia
- Whistling face syndrome, recessive form
- Whistling face-windmill vane hand syndrome
- Whitaker syndrome
- White forelock (poliosis) syndrome with multiple congenital malformations
- White forelock and leukoderma with neurological impairment
- White forelock with malformations
- White liver disease
- White matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome
- White platelet syndrome
- White sponge nevus of cannon
- Whitmore disease
- WHO Grade II Ependymal Neoplasm
- Whooping cough
- WHS
- Whyte Murphy syndrome
- Whyte Petersen McAlister syndrome
- Whyte syndrome
- Widened medullary cavities of bone, aortic calcification, abnormal dentition, and muscular weakness
- Wieacker syndrome
- Wieacker Wolff syndrome
- Wiedemann Grosse Dibbern syndrome
- Wiedemann Oldigs Oppermann syndrome
- Wiedemann Rautenstrauch syndrome
- Wiedemann-Beckwith Syndrome (WBS)
- Wiedemann-Oldigs-Oppermann syndrome
- Wiedemann-Rautenstrauch syndrome
- Wiedemann-Steiner syndrome
- Wildervanck syndrome
- Wildervanck-Smith syndrome
- Wilkie syndrome
- Willebrand disease, acquired
- Williams syndrome
- Williams-Beuren region duplication syndrome
- Williams-Beuren syndrome
- Willi-Prader syndrome
- Willis Ekbom disease- not a rare disease.
- Wilms' tumor
- Wilms tumor 5
- Wilms tumor and pseudohermaphroditism
- Wilms tumor and radial bilateral aplasia
- Wilms tumor, Aniridia, Genitourinary anomalies, mental Retardation syndrome
- Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome
- Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation syndrome
- Wilson disease
- Wilson Turner mental retardation syndrome (formerly)
- Wilson-Mikity syndrome
- Wilson-Turner syndrome
- Winchester disease
- Winchester syndrome
- Winchester-Grossman Syndrome
- Windblown hand
- Windswept hand
- Winged helix deficiency
- Winkelmann-Bethge-Pfeiffer syndrome
- Winship-Viljoen-Leary syndrome
- Winter Harding Hyde syndrome
- Wisconsin syndrome
- Wiskott Aldrich syndrome
- Witkop syndrome
- Wittwer syndrome
- WL syndrome
- WM Syndrome
- WMS
- WMS
- WND
- WNS
- Wolcott Rallison syndrome
- Wolf syndrome
- Wolffian adenoma
- Wolffian adnexal tumor
- Wolffian tumor
- Wolff-Parkinson-White syndrome- not a rare disease.
- Wolf-Hirschhorn syndrome
- Wolfram syndrome
- Wolman disease
- Woodhouse Sakati syndrome
- Woodhouse-Sakati syndrome
- Woods Black Norbury syndrome
- Wool sorter's disease
- Woolly hair
- Woolly hair hypotrichosis everted lower lip and outstanding ears
- Woolly hair palmoplantar keratoderma cardiac abnormalities
- Woolly hair syndrome
- Woolly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome
- Woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
- Wooly hair - palmoplantar keratoderma - dilated cardiomyopathy
- Wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome
- Wooly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome
- Worm infections
- Worster Drought syndrome
- Worth syndrome
- Worth type autosomal dominant osteosclerosis
- Wound botulism (subtype)
- WPW syndrome- not a rare disease.
- Wrinkly skin syndrome
- WRN
- WS 2
- WS type 2
- WS1
- WS2A
- WS2B
- WS3
- WS4
- WSN
- WSN
- WSS
- WT limb blood syndrome
- WT syndrome
- WT1
- WT5
- WTS
- Wuchereria Bancrofti infection
- Wuchereriasis
- WWS
- Wyburn Mason syndrome
- Wyburn-Mason syndrome
- WZS
NIH genetic and rare disease info
List of rare diseases-W is a rare disease.
Rare and genetic diseases | ||||||
---|---|---|---|---|---|---|
Rare diseases - List of rare diseases-W
|
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