Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C3280303
Disease: Abnormal hair whorl
Abnormal hair whorl 		5 0 1 0.20 0 0
CUI: C0002170
Disease: Alopecia
Alopecia 		491 0 1 2.0E-03 0 0
CUI: C0002171
Disease: Alopecia Areata
Alopecia Areata 		114 0 1 8.8E-03 0 0
CUI: C0236018
Disease: Aura
Aura 		83 0 1 1.2E-02 0 0
CUI: C0751111
Disease: Awakening Epilepsy
Awakening Epilepsy 		83 0 1 1.2E-02 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		595 0 1 1.7E-03 0 0
CUI: C0221357
Disease: Brachydactyly
Brachydactyly 		325 0 1 3.1E-03 0 0
CUI: C0006111
Disease: Brain Diseases
Brain Diseases 		345 0 1 2.9E-03 0 0
CUI: C1859690
Disease: CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME
CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME 		5 0 1 0.20 0 0
CUI: C2675370
Disease: Capillary Malformation Without Arteriovenous Malformation
Capillary Malformation Without Arteriovenous Malformation 		2 0 1 0.50 0 0
CUI: C1842180
Disease: CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder)
CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION (disorder) 		22 0 1 4.5E-02 0 0
CUI: C1864186
Disease: CDAGS SYNDROME
CDAGS SYNDROME 		1 0 1 1.00 0 0
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy 		454 0 1 2.2E-03 0 0
CUI: C0085996
Disease: Child Development Deviations
Child Development Deviations 		29 0 1 3.4E-02 0 0
CUI: C0085997
Disease: Child Development Disorders, Specific
Child Development Disorders, Specific 		30 0 1 3.3E-02 0 0
CUI: C0008925
Disease: Cleft Palate
Cleft Palate 		611 0 1 1.6E-03 0 0
CUI: C4551485
Disease: Clinodactyly
Clinodactyly 		148 0 1 6.8E-03 0 0
CUI: C0265610
Disease: Clinodactyly of fingers
Clinodactyly of fingers 		160 0 1 6.3E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		112 0 1 8.9E-03 0 0
CUI: C0008073
Disease: Developmental Disabilities
Developmental Disabilities 		355 0 1 2.8E-03 0 0
CUI: C0085584
Disease: Encephalopathies
Encephalopathies 		457 0 1 2.2E-03 0 0
CUI: C0014544
Disease: Epilepsy
Epilepsy 		1215 0 1 8.2E-04 0 0
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic 		88 0 1 1.1E-02 0 0
CUI: C0015544
Disease: Failure to Thrive
Failure to Thrive 		842 0 1 1.2E-03 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		73 0 1 1.4E-02 0 0