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: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		63 92 16 7.7E-02 15 4.6E-02
CUI: C1844806
Disease: Weight less than 3rd percentile
Weight less than 3rd percentile 		22 27 13 7.7E-02 17 6.6E-02
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger 		37 39 14 7.7E-02 8 2.9E-02
CUI: C0027092
Disease: Myopia
Myopia 		45 52 14 7.3E-02 7 2.4E-02
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		46 66 14 7.3E-02 13 4.3E-02
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		21 27 12 7.1E-02 11 4.2E-02
CUI: C0013421
Disease: Dystonia
Dystonia 		42 61 13 6.9E-02 10 3.4E-02
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		28 54 12 6.8E-02 18 6.4E-02
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		33 50 12 6.6E-02 13 4.6E-02
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		19 20 11 6.5E-02 7 2.7E-02
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		37 49 12 6.5E-02 6 2.1E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 69 13 6.5E-02 8 2.6E-02
CUI: C0029453
Disease: Osteopenia
Osteopenia 		23 23 11 6.4E-02 10 3.9E-02
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk 		25 25 11 6.3E-02 8 3.0E-02
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		44 58 12 6.2E-02 6 2.0E-02
CUI: C0856975
Disease: Autistic behavior
Autistic behavior 		44 76 12 6.2E-02 5 1.6E-02
CUI: C0028738
Disease: Nystagmus
Nystagmus 		62 83 13 6.2E-02 11 3.5E-02
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive 		63 77 13 6.2E-02 11 3.5E-02
CUI: C0016202
Disease: Flatfoot
Flatfoot 		30 38 11 6.1E-02 6 2.2E-02
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		30 35 11 6.1E-02 7 2.6E-02
CUI: C0014877
Disease: Esotropia
Esotropia 		33 38 11 6.0E-02 10 3.6E-02
CUI: C3553450
Disease: Profound global developmental delay
Profound global developmental delay 		17 19 10 6.0E-02 9 3.5E-02
CUI: C0151526
Disease: Premature Birth
Premature Birth 		35 40 11 6.0E-02 6 2.1E-02
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		36 46 11 5.9E-02 11 3.9E-02
CUI: C0026106
Disease: Mild Mental Retardation
Mild Mental Retardation 		39 48 11 5.9E-02 3 1.0E-02