Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/11
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- UDP-galactose-4-epimerase deficiency
- Ulbright Hodes syndrome
- Ulerythema ophryogenesis
- Ulna and fibula absence with severe limb deficit
- Ulna hypoplasia mental retardation
- Ulna metaphyseal dysplasia syndrome
- Ulnar hypoplasia lobster claw deformity of feet
- Umbilical cord ulceration intestinal atresia
- Uncombable hair syndrome
- Uniparental disomy of 11
- Uniparental disomy of 13
- Uniparental disomy of 14
- Uniparental disomy of 2
- Uniparental disomy of 6
- Unna-Politzer nevus
- Unna's seborrhoeic eczema
- Upington disease
- Upper limb defect eye and ear abnormalities
- Upton Young syndrome
- Urachal cancer
- Urachal cyst
- Uramoron syndrome
- Urban Rogers Meyer syndrome
- Urban Schosser Spohn syndrome
- Urea cycle enzymopathies
- Urethral obstruction sequence
- Urioste Martinez Frias syndrome
- Urocanase deficiency
- Urogenital adysplasia
- Urophathy distal obstructive polydactyly
- Urticaria-deafness-amyloidosis
- VACTERL association with hydrocephaly, X linked
- VACTERL hydrocephaly
- Vacuolar myopathy
- Vagina absence of
- Vagneur Triolle Ripert syndrome
- Valinemia
- Valproic acid antenatal infection
- Valvular dysplasia of the child
- Van Allen Myhre syndrome
- Van Bogaert-Hozay syndrome
- Van De Berghe Dequeker syndrome
- Van Den Bosch syndrome
- Van Den Ende Brunner syndrome
- Van der Woude syndrome 2
- Van Maldergem Wetzburger Verloes syndrome
- Van Regemorter Pierquin Vamos syndrome
- Varadi Papp syndrome
- Vas deferens, congenital bilateral aplasia of
- Vascular disruption sequence
- Vascular helix of umbilical cord
- Vascular malformations of the brain
- Vascular malposition
- Vasculitis hypersensitivity
- Vasculitis, cutaneous necrotizing
- Vasopressin-resistant diabetes insipidus
- Vasquez Hurst Sotos syndrome
- Vein of Galen aneurysmal dilatation
- Vein of Galen aneurysmal malformation
- Velofacioskeletal syndrome
- Velopharyngeal incompetence
- Venencie Powell Winkelmann syndrome
- Ventricular extrasystoles perodactyly Robin sequence
- Ventricular familial preexcitation syndrome
- Ventriculo-arterial discordance, isolated
- Ventruto Digirolamo Festa syndrome
- Verloes Bourguignon syndrome
- Verloes David syndrome
- Verloes Gillerot Fryns syndrome
- Verloes Van Maldergem Marneffe syndrome
- Verloove Vanhorick Brubakk syndrome
- Verrucous nevus acanthokeratolytic
- Verrucous nevus
- Vertebral body fusion overgrowth
- Vertebral fusion posterior lumbosacral blepharoptosis
- Vertical talus
- Vestibulocochlear dysfunction progressive familial
- Viljoen Kallis Voges syndrome
- Viljoen Smart syndrome
- Viljoen Winship syndrome
- Virilism
- Virilizing ovarian tumor
- Virus associated hemophagocytic syndrome
- Visceral myopathy familial external ophthalmoplegia
- Visceral steatosis
- Viscero-atrial heterotaxia
- Visna Maedi complex
- Vitamin A embryopathy
- Vitamin B 6 Deficiency
- Vitamin B12 responsive methylmalonic acidemia, cbl A
- Vitamin B12 responsive methylmalonicaciduria
- Vitamin D resistant rickets
- Vitamin E familial isolated, deficiency of
- Vitiligo mental retardation facial dysmorphism uremia
- Vitiligo psychomotor retardation cleft palate facial dysmorphism
- Vitreoretinal degeneration
- Vitreoretinochoroidopathy dominant
- Vocal cord dysfunction familial
- Von Voss Cherstvoy syndrome
- Vulvovaginitis
- W syndrome
- Waaler Aarskog 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 type Pierpont
- Wagner-Stickler syndrome
- Walbaum Titran Durieux Crepin syndrome
- Waldmann disease
- Walker Dyson syndrome
- Wallis Zieff Goldblatt syndrome
- Wandering spleen
- Warburg Sjo Fledelius syndrome
- Warburg Thomsen syndrome
- Warburton Anyane Yeboa syndrome
- Warfarin antenatal infection
- Warman Mulliken Hayward syndrome
- Warm-reacting-antibody hemolytic anemia
- Watson syndrome
- Weaver Johnson syndrome
- Weaver like syndrome
- Weaver syndrome
- Weaver Williams syndrome
- Weber Parkes syndrome
- Weber Sturge Dimitri syndrome
- Webster Deming syndrome
- Wegmann Jones Smith syndrome
- Weil syndrome
- Weinstein Kliman Scully syndrome
- Weismann Netter Stuhl syndrome
- Welander distal myopathy, Swedish type
- Weleber Hecht Bigley syndrome
- Wellesley Carmen French syndrome
- Wells Jankovic syndrome
- Wells syndrome
- Wernicke Korsakoff syndrome
- Westerhof Beemer Cormane syndrome
- Western equine encephalitis
- Westphall disease
- Wheat Hypersensitivity
- Whitaker syndrome
- White matter hypoplasia corpus callosum agenesia mental retardation
- White sponge nevus of cannon
- Whyte Murphy syndrome
- Wieacker syndrome
- Wiedemann Grosse Dibbern syndrome
- Wiedemann Oldigs Oppermann syndrome
- Wiedemann Opitz syndrome
- Wiedemann Rautenstrauch syndrome
- Wildervanck syndrome
- Wilkes Stevenson syndrome
- Wilkie Taylor Scambler syndrome
- Willems De vries syndrome
- Wilms tumor and pseudohermaphroditism
- Wilms tumor radial bilateral aplasia
- Wilson Turner syndrome
- Winchester syndrome
- Winkelman Bethge Pfeiffer syndrome
- Winship Viljoen Leary syndrome
- Winter Harding Hyde syndrome
- Winter Shortland Temple syndrome
- Wisconsin syndrome
- Witkop syndrome
- Wohlwill-Andrade syndrome
- Wolcott-Rallison syndrome
- Woodhouse Sakati syndrome
- Woods Black Norbury syndrome
- Woods Leversha Rogers syndrome
- Woolly hair - autosomal recessive
- Woolly hair autosomal recessive
- Woolly hair hypotrichosis everted lower lip outstanding ears
- Woolly hair palmoplantar keratoderma cardiac anomalies
- Woolly hair, congenital
- Wooly hair autosomal recessive
- Worth syndrome
- Wright Dick syndrome
- Wrinkly skin syndrome
- Wt limb blood syndrome
- Wyburn-Mason's syndrome
- X chromosome, duplication Xq13 1 q21 1
- X chromosome, monosomy Xp22 pter
- X chromosome, monosomy Xq28
- X chromosome, trisomy Xp3
- X chromosome, trisomy Xpter Xq13
- X chromosome, trisomy Xq
- X chromosome, trisomy Xq25
- X fragile site folic acid type
- Xanthic urolithiasis
- Xanthine oxydase deficiency
- Xanthomatosis cerebrotendinous
- Xerocytosis, hereditary
- Xeroderma pigmentosum, type 1
- Xeroderma pigmentosum, type 2
- Xeroderma pigmentosum, type 3
- Xeroderma pigmentosum, type 5
- Xeroderma pigmentosum, type 6
- Xeroderma pigmentosum, type 7
- Xeroderma pigmentosum, variant type
- Xeroderma talipes enamel defects
- Xk aprosencephaly
- X-linked juvenile retinoschisis
- X-linked lymphoproliferative syndrome
- X-linked mental retardation and macro-orchidism
- X-linked mental retardation associated with marXq2
- X-linked mental retardation Brooks type
- X-linked mental retardation craniofacial abnormal microcephaly club
- X-linked mental retardation De silva type
- X-linked mental retardation Hamel type
- X-linked mental retardation type Gustavson
- X-linked mental retardation type Martinez
- X-linked mental retardation type Raynaud
- X-linked mental retardation type Schutz
- X-linked mental retardation type Snyder
- X-linked mental retardation type Wittner
- X-linked mental retardation-hypotonia
- X-linked trait
- XY gonadal agenesis syndrome
- Y chromosome deletions
- Yim Ebbin syndrome
- Yorifuji Okuno syndrome
- Yoshimura-Takeshita syndrome
- Young Hugues syndrome
- Young Maders syndrome
- Young Mc keever Squier syndrome
- Young Simpson syndrome
- Young Syndrome
- Yunis Varon syndrome
- Yusho Disease
- Zazam Sheriff Phillips syndrome
- Zimmerman Laband syndrome
- Zlotogora syndrome
- Zonular cataract and nystagmus
- Zori Stalker Williams syndrome
- Zunich-Kaye syndrome
