|
XPA
(HGNC:12814)
|
xeroderma pigmentosum group A
(MONDO_0010210)
|
Definitive
|
|
|
WWOX
(HGNC:12799)
|
developmental and epileptic encephalopathy
(MONDO_0100062)
|
Strong
|
|
|
WWOX
(HGNC:12799)
|
developmental and epileptic encephalopathy, 28
(MONDO_0014533)
|
Strong
|
|
|
WT1
(HGNC:12796)
|
Denys-Drash syndrome
(MONDO_0008682)
|
Definitive
|
|
|
WWOX
(HGNC:12799)
|
autosomal recessive spinocerebellar ataxia 12
(MONDO_0013687)
|
Moderate
|
|
|
WT1
(HGNC:12796)
|
Frasier syndrome
(MONDO_0007635)
|
Definitive
|
|
|
WRN
(HGNC:12791)
|
Werner syndrome
(MONDO_0010196)
|
Definitive
|
|
|
WRN
(HGNC:12791)
|
osteosarcoma
(MONDO_0009807)
|
Limited
|
|
|
WNT7A
(HGNC:12786)
|
Fuhrmann syndrome
(MONDO_0009232)
|
Moderate
|
|
|
WNT7A
(HGNC:12786)
|
phocomelia, Schinzel type
(MONDO_0010164)
|
Moderate
|
|
|
WNT5A
(HGNC:12784)
|
autosomal dominant Robinow syndrome
(MONDO_0008389)
|
Strong
|
|
|
WNT10B
(HGNC:12775)
|
split hand-foot malformation 6
(MONDO_0009157)
|
Moderate
|
|
|
WNT10B
(HGNC:12775)
|
tooth agenesis
(MONDO_0005486)
|
Moderate
|
|
|
WNT1
(HGNC:12774)
|
osteogenesis imperfecta type 15
(MONDO_0014086)
|
Strong
|
|
|
NSD2
(HGNC:12766)
|
Rauch-Steindl syndrome
(MONDO_0859219)
|
Strong
|
|
|
WFS1
(HGNC:12762)
|
Wolfram syndrome
(MONDO_0018105)
|
Definitive
|
|
|
FOXN1
(HGNC:12765)
|
T-cell immunodeficiency, congenital alopecia, and nail dystrophy
(MONDO_0011132)
|
Strong
|
|
|
WFS1
(HGNC:12762)
|
Wolfram-like syndrome
(MONDO_0013673)
|
Strong
|
|
|
WFS1
(HGNC:12762)
|
Wolfram syndrome 1
(MONDO_0009101)
|
Definitive
|
|
|
WFS1
(HGNC:12762)
|
type 2 diabetes mellitus
(MONDO_0005148)
|
Strong
|
|