Stats

Total associations
6699
Unique genes
4252
Unique diseases
3300
Gene–disease association summaries
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Gene–Disease Browser

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Gene Disease Score Actions
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
Showing 3641–3660 of 6699