Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/11

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 * 1) Ulna metaphyseal dysplasia syndrome
 * 2) Unna-Politzer nevus
 * 3) Upper limb defect eye and ear abnormalities
 * 4) Urethral obstruction sequence
 * 5) Urophathy distal obstructive polydactyly
 * 6) VACTERL association with hydrocephaly, X linked
 * 7) VACTERL hydrocephaly
 * 8) Vagneur Triolle Ripert syndrome
 * 9) Van Allen Myhre syndrome
 * 10) Van Bogaert-Hozay syndrome
 * 11) Van Regemorter Pierquin Vamos syndrome
 * 12) Vascular disruption sequence
 * 13) Vascular helix of umbilical cord
 * 14) Vascular malposition
 * 15) Velofacioskeletal syndrome
 * 16) Verloes Bourguignon syndrome
 * 17) Verloes David syndrome
 * 18) Verloes Gillerot Fryns syndrome
 * 19) Verloove Vanhorick Brubakk syndrome
 * 20) Verrucous nevus acanthokeratolytic
 * 21) Verrucous nevus
 * 22) Vestibular paroxysmia
 * 23) Vertebral body fusion overgrowth
 * 24) Vertebral fusion posterior lumbosacral blepharoptosis
 * 25) Viljoen Winship syndrome
 * 26) Virilizing ovarian tumor
 * 27) Virus associated hemophagocytic syndrome
 * 28) Vitiligo mental retardation facial dysmorphism uremia
 * 29) Vitiligo psychomotor retardation cleft palate facial dysmorphism
 * 30) Vitreoretinal degeneration
 * 31) W syndrome
 * 32) Waaler Aarskog syndrome
 * 33) Walbaum Titran Durieux Crepin syndrome
 * 34) Walker Dyson syndrome
 * 35) Warburton Anyane Yeboa syndrome
 * 36) Weaver Johnson syndrome
 * 37) Weaver Williams syndrome
 * 38) Webster Deming syndrome
 * 39) Wegmann Jones Smith syndrome
 * 40) Weinstein Kliman Scully syndrome
 * 41) Weleber Hecht Bigley syndrome
 * 42) Wellesley Carmen French syndrome
 * 43) Whyte Murphy syndrome
 * 44) Wiedemann Oldigs Oppermann syndrome
 * 45) Winkelman Bethge Pfeiffer syndrome
 * 46) Winship Viljoen Leary syndrome
 * 47) Winter Harding Hyde syndrome
 * 48) Wisconsin syndrome
 * 49) Woods Black Norbury syndrome
 * 50) Woods Leversha Rogers syndrome
 * 51) Wright Dick syndrome
 * 52) Wt limb blood syndrome
 * 53) X chromosome, duplication Xq13 1 q21 1
 * 54) X chromosome, monosomy Xp22 pter
 * 55) X chromosome, monosomy Xq28
 * 56) X chromosome, trisomy Xp3
 * 57) X chromosome, trisomy Xpter Xq13
 * 58) X chromosome, trisomy Xq
 * 59) X chromosome, trisomy Xq25
 * 60) X fragile site folic acid type
 * 61) Xerocytosis, hereditary
 * 62) Xeroderma talipes enamel defects
 * 63) Yorifuji Okuno syndrome
 * 64) Yoshimura-Takeshita syndrome