|
BRWD1
(HGNC:12760)
|
primary ciliary dyskinesia
(MONDO_0016575)
|
Limited
|
|
|
WASF1
(HGNC:12732)
|
neurodevelopmental disorder with absent language and variable seizures
(MONDO_0032876)
|
Strong
|
|
|
WDR4
(HGNC:12756)
|
Galloway-Mowat syndrome
(MONDO_0009627)
|
Limited
|
|
|
WIPF1
(HGNC:12736)
|
Wiskott-Aldrich syndrome
(MONDO_0010518)
|
Limited
|
|
|
WAS
(HGNC:12731)
|
thrombocytopenia 1
(MONDO_0010743)
|
Definitive
|
|
|
WAS
(HGNC:12731)
|
Wiskott-Aldrich syndrome
(MONDO_0010518)
|
Definitive
|
|
|
WARS2
(HGNC:12730)
|
neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures
(MONDO_0060578)
|
Strong
|
|
|
WARS2
(HGNC:12730)
|
mitochondrial disease
(MONDO_0044970)
|
Strong
|
|
|
WARS1
(HGNC:12729)
|
distal hereditary motor neuropathy
(MONDO_0018894)
|
Moderate
|
|
|
VWF
(HGNC:12726)
|
von Willebrand disease type 2N
(MONDO_0015631)
|
Definitive
|
|
|
VWF
(HGNC:12726)
|
von Willebrand disease type 2M
(MONDO_0015630)
|
Strong
|
|
|
VWF
(HGNC:12726)
|
von Willebrand disease type 2B
(MONDO_0015629)
|
Definitive
|
|
|
VWF
(HGNC:12726)
|
von Willebrand disease type 2A
(MONDO_0015628)
|
Definitive
|
|
|
VWF
(HGNC:12726)
|
von Willebrand disease 2
(MONDO_0013304)
|
Definitive
|
|
|
BEST1
(HGNC:12703)
|
retinitis pigmentosa 50
(MONDO_0013175)
|
Limited
|
|
|
VWF
(HGNC:12726)
|
von Willebrand disease 3
(MONDO_0010191)
|
Definitive
|
|
|
VWF
(HGNC:12726)
|
von Willebrand disease 1
(MONDO_0008668)
|
Definitive
|
|
|
VSX1
(HGNC:12723)
|
posterior polymorphous corneal dystrophy
(MONDO_0020364)
|
Disputed
|
|
|
VRK1
(HGNC:12718)
|
pontocerebellar hypoplasia type 1
(MONDO_0016396)
|
Moderate
|
|
|
VPS33B
(HGNC:12712)
|
arthrogryposis, renal dysfunction, and cholestasis 1
(MONDO_0008822)
|
Definitive
|
|