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W
Disorder Name	Genes	Alternate Names	OMIM	Inheritance
Waardenburg Syndrome, Type 2	SOX10, MITF, SNAI2	Waardenburg syndrome without dystopia canthorum, WS2	193510, 600193, 606662, 608890, 611584, 103470	autosomal dominant
Waardenburg Syndrome, Type 3	PAX3	Klein-Waardenburg syndrome, Waardenburg syndrome with upper limb anomalies	148820	autosomal dominant, autosomal recessive?
Waardenburg Syndrome, Type 4	SOX10, EDNRB	Waardenburg-Shah syndrome, WS4, Waardenburg syndrome with Hirschsprung disease	277580, 613265, 613266	autosomal recessive, autosomal dominant
Wagner Syndrome	VCAN	WGN1, Wagner vitreoretinal degeneration, erosive vitreoretinopathy, ERVR	143200	autosomal dominant
Walker-Warburg Syndrome	POMT1, POMT2, POMGNT1, FKTN, FKRP, LARGE	COD-MD syndrome, WWS, dystroglycanopathy, MDDG, HARD syndrome, MEB	236670	autosomal recessive
Watson Syndrome	NF1	pulmonic stenosis with cafe-au-lait spots	193520	autosomal dominant
Weill-Marchesani Syndrome 1	ADAMTS10	WM syndrome, WMS1, autosomal recessive Weill-Marchesani syndrome	277600	autosomal recessive
Weill-Marchesani Syndrome 2	FBN1	glaucoma-lens ectopia-microspherophakia-stiffness-shortness syndrome, Weill-Marchesani syndrome 2, WMS2, GEMSS	608328	autosomal dominant
Weill-Marchesani-Like Syndrome	ADAMTS17		613195	autosomal recessive
Wildervanck Syndrome	?	cervicooculoacoustic syndrome	314600	?
Williams Syndrome	ELN	WMS, Williams-Beuren syndrome, WBS	194050	deletion syndrome
Wilson Disease	ATP7B	hepatolenticular degeneration, WD	277900	autosomal recessive
Wolfram Syndrome 1	WFS1	WFS1, WFS, DIDMOAD	222300	autosomal recessive
Wolfram Syndrome 2	CISD2	DIDMOAD, WFS2	604928	autosomal recessive

Z
Disorder Name	Genes	Alternate Names	OMIM	Inheritance
ZTTK Syndrome	SON	ZTTKS, Zhu-Tokita-Takenouchi-Kim syndrome, Tokita-Kim Syndrome	617140	autosomal dominant