Source: GENOMICS_ENGLAND

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
Congenital ocular coloboma (disorder) 		disease 0.400 limited 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C4025860
Disease: Hearing abnormality
Hearing abnormality 		disease 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C4022810
Disease: Abnormality of nervous system morphology
Abnormality of nervous system morphology 		disease 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system 		disease 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C2677504
Disease: AUTISM, SUSCEPTIBILITY TO, 15
AUTISM, SUSCEPTIBILITY TO, 15 		disease 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		disease 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C0344559
Disease: Irido-corneo-trabecular dysgenesis (disorder)
Irido-corneo-trabecular dysgenesis (disorder) 		disease 0.300 limited 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C0266544
Disease: Microcornea
Microcornea 		disease 0.300 limited 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C0243050
Disease: Cardiovascular Abnormalities
Cardiovascular Abnormalities 		group 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C0042063
Disease: Urogenital Abnormalities
Urogenital Abnormalities 		group 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C0036572
Disease: Seizures
Seizures 		phenotype 0.300 strong 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		phenotype 0.300 limited 1.000 1 0 2019 2019
Entrez Id: 22884
Gene Symbol: WDR37
WDR37 		WD repeat domain 37 0.751 0.231 0.57
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye 		phenotype 0.300 strong 1.000 1 0 2019 2019