Disorders: W

Disorders Alternate Names Genes Inheritance Pattern
Waardenburg Syndrome, Type 1 Klein-Waardenburg syndrome, Waardenburg syndrome with dystopia canthorum, WS1 PAX3 autosomal dominant
Waardenburg Syndrome, Type 2 Waardenburg syndrome without dystopia canthorum, WS2 MITF, SNAI2, SOX10 autosomal dominant
Waardenburg Syndrome, Type 3 Klein-Waardenburg syndrome, Waardenburg syndrome with upper limb anomalies PAX3 autosomal dominant, autosomal recessive?
Waardenburg Syndrome, Type 4 Waardenburg syndrome with Hirschsprung disease, Waardenburg-Shah syndrome, WS4 EDNRB, SOX10 autosomal dominant, autosomal recessive
Wagner Syndrome erosive vitreoretinopathy, ERVR, Wagner vitreoretinal degeneration, WGN1 VCAN autosomal dominant
Walker-Warburg Syndrome COD-MD syndrome, dystroglycanopathy, HARD syndrome, MDDG, MEB, WWS FKRP, FKTN, LARGE, POMGNT1, POMT1, POMT2 autosomal recessive
Warburg Micro Syndrome 1 micro syndrome, WARBM1 RAB3GAP1 autosomal recessive
Watson Syndrome pulmonic stenosis with cafe-au-lait spots NF1 autosomal dominant
Weill-Marchesani Syndrome 1 autosomal recessive Weill-Marchesani syndrome, WM syndrome, WMS1 ADAMTS10 autosomal recessive
Weill-Marchesani Syndrome 2 GEMSS, glaucoma-lens ectopia-microspherophakia-stiffness-shortness syndrome, Weill-Marchesani syndrome 2, WMS2 FBN1 autosomal dominant
Weill-Marchesani-Like Syndrome ADAMTS17 autosomal recessive
Wildervanck Syndrome cervicooculoacoustic syndrome ? ?
Williams Syndrome WBS, Williams-Beuren syndrome, WMS ELN deletion syndrome
Wilson Disease hepatolenticular degeneration, WD ATP7B autosomal recessive
Wolfram Syndrome 1 DIDMOAD, WFS, WFS1 WFS1 autosomal recessive
Wolfram Syndrome 2 DIDMOAD, WFS2 CISD2 autosomal recessive