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 |
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 |