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: C0155380
Disease: Dissociated Nystagmus
Dissociated Nystagmus 		1 0 1 0.20 0 0
CUI: C0265974
Disease: Birthmark
Birthmark 		1 0 1 0.20 0 0
CUI: C0266094
Disease: Congenital macrocheilia
Congenital macrocheilia 		1 0 1 0.20 0 0
CUI: C0267024
Disease: Hypertrophy of lip
Hypertrophy of lip 		1 0 1 0.20 0 0
CUI: C0271383
Disease: Symptomatic Nystagmus
Symptomatic Nystagmus 		1 0 1 0.20 0 0
CUI: C0271384
Disease: Spontaneous Ocular Nystagmus
Spontaneous Ocular Nystagmus 		1 0 1 0.20 0 0
CUI: C0271387
Disease: Rebound Nystagmus
Rebound Nystagmus 		1 0 1 0.20 0 0
CUI: C0271389
Disease: Jerk Nystagmus
Jerk Nystagmus 		1 0 1 0.20 0 0
CUI: C0332972
Disease: Congenital vascular proliferation
Congenital vascular proliferation 		1 0 1 0.20 0 0
CUI: C0339541
Disease: Goldmann-Favre syndrome (disorder)
Goldmann-Favre syndrome (disorder) 		1 0 1 0.20 0 0
CUI: C0349623
Disease: Primary Melanocytic Lesion of Meninges
Primary Melanocytic Lesion of Meninges 		1 0 1 0.20 0 0
CUI: C0520731
Disease: Retraction Nystagmus
Retraction Nystagmus 		1 0 1 0.20 0 0
CUI: C0521753
Disease: Temporary Nystagmus
Temporary Nystagmus 		1 0 1 0.20 0 0
CUI: C0521754
Disease: Permanent Nystagmus
Permanent Nystagmus 		1 0 1 0.20 0 0
CUI: C0521755
Disease: Unidirectional Nystagmus
Unidirectional Nystagmus 		1 0 1 0.20 0 0
CUI: C0521756
Disease: Multidirectional Nystagmus
Multidirectional Nystagmus 		1 0 1 0.20 0 0
CUI: C0521757
Disease: Conjugate Nystagmus
Conjugate Nystagmus 		1 0 1 0.20 0 0
CUI: C0521759
Disease: Convergence Nystagmus
Convergence Nystagmus 		1 0 1 0.20 0 0
CUI: C0521760
Disease: Fatigable Positional Nystagmus
Fatigable Positional Nystagmus 		1 0 1 0.20 0 0
CUI: C0521761
Disease: Non-Fatigable Positional Nystagmus
Non-Fatigable Positional Nystagmus 		1 0 1 0.20 0 0
CUI: C0522035
Disease: Edema of the upper extremity
Edema of the upper extremity 		1 1 1 0.20 1 0.20
CUI: C1838876
Disease: MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE
MITOCHONDRIAL MYOPATHY, LETHAL, INFANTILE 		1 0 1 0.20 0 0
CUI: C1970163
Disease: RETINITIS PIGMENTOSA 37 (disorder)
RETINITIS PIGMENTOSA 37 (disorder) 		1 6 1 0.20 1 1.0E-01
CUI: C2750720
Disease: Cone-Rod Dystrophy 13
Cone-Rod Dystrophy 13 		1 0 1 0.20 0 0
CUI: C2931029
Disease: Nevi flammei, familial multiple
Nevi flammei, familial multiple 		1 0 1 0.20 0 0