Source: CLINVAR ×
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: C0014877
Disease: Esotropia
Esotropia 		33 38 25 8.0E-02 21 4.0E-02
CUI: C1849265
Disease: Overgrowth
Overgrowth 		81 93 28 7.9E-02 4 6.7E-03
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		46 66 25 7.7E-02 22 4.0E-02
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		63 77 26 7.6E-02 24 4.3E-02
CUI: C0009806
Disease: Constipation
Constipation 		40 49 24 7.5E-02 18 3.4E-02
CUI: C0013421
Disease: Dystonia
Dystonia 		42 61 23 7.1E-02 19 3.5E-02
CUI: C0036857
Disease: Severe intellectual disability
Severe intellectual disability 		43 62 23 7.1E-02 13 2.3E-02
CUI: C0027092
Disease: Myopia
Myopia 		45 52 23 7.1E-02 17 3.1E-02
CUI: C0037317
Disease: Sleep disturbances
Sleep disturbances 		37 41 22 6.9E-02 14 2.6E-02
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		37 39 22 6.9E-02 16 3.0E-02
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		39 59 22 6.9E-02 27 5.0E-02
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		44 76 21 6.4E-02 22 3.9E-02
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		29 30 20 6.4E-02 18 3.5E-02
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		35 47 20 6.3E-02 18 3.4E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		39 51 20 6.2E-02 16 3.0E-02
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		28 54 19 6.1E-02 17 3.1E-02
CUI: C0016202
Disease: Flatfoot
Flatfoot 		30 38 18 5.7E-02 12 2.3E-02
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		31 34 18 5.7E-02 10 1.9E-02
CUI: C0456070
Disease: Growth delay
Growth delay 		31 40 18 5.7E-02 15 2.8E-02
CUI: C0423110
Disease: Downward slant of palpebral fissure
Downward slant of palpebral fissure 		35 49 18 5.6E-02 14 2.6E-02
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		37 94 18 5.6E-02 8 1.4E-02
CUI: C0038273
Disease: Stereotypic Movement Disorder
Stereotypic Movement Disorder 		21 25 17 5.5E-02 12 2.3E-02
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		25 25 17 5.5E-02 12 2.3E-02
CUI: C1837142
Disease: Poor suck
Poor suck 		28 31 17 5.4E-02 15 2.9E-02
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		37 49 17 5.3E-02 13 2.4E-02