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 3.4E-02 0 0
CUI: C0233283
Disease: Complete breech presentation
Complete breech presentation
1 1 1 3.4E-02 1 2.4E-02
CUI: C0234918
Disease: Morbilliform rash
Morbilliform rash
1 0 1 3.4E-02 0 0
CUI: C0271383
Disease: Symptomatic Nystagmus
Symptomatic Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0271384
Disease: Spontaneous Ocular Nystagmus
Spontaneous Ocular Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0271387
Disease: Rebound Nystagmus
Rebound Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0271389
Disease: Jerk Nystagmus
Jerk Nystagmus
1 0 1 3.4E-02 0 0
Other congenital malformation syndromes with other skeletal changes
1 0 1 3.4E-02 0 0
CUI: C0520731
Disease: Retraction Nystagmus
Retraction Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0521753
Disease: Temporary Nystagmus
Temporary Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0521754
Disease: Permanent Nystagmus
Permanent Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0521755
Disease: Unidirectional Nystagmus
Unidirectional Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0521756
Disease: Multidirectional Nystagmus
Multidirectional Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0521757
Disease: Conjugate Nystagmus
Conjugate Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0521759
Disease: Convergence Nystagmus
Convergence Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0521760
Disease: Fatigable Positional Nystagmus
Fatigable Positional Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0521761
Disease: Non-Fatigable Positional Nystagmus
Non-Fatigable Positional Nystagmus
1 0 1 3.4E-02 0 0
CUI: C0854297
Disease: Head deformity
Head deformity
1 0 1 3.4E-02 0 0
Hyper-IgD periodic fever syndrome (HIDS)
1 0 1 3.4E-02 0 0
CUI: C1442958
Disease: Actinic porokeratosis
Actinic porokeratosis
1 0 1 3.4E-02 0 0
CUI: C1835875
Disease: Normocytic hypoplastic anemia
Normocytic hypoplastic anemia
1 0 1 3.4E-02 0 0
CUI: C1835881
Disease: Fluctuating hepatomegaly
Fluctuating hepatomegaly
1 0 1 3.4E-02 0 0
CUI: C1835882
Disease: Fluctuating splenomegaly
Fluctuating splenomegaly
1 0 1 3.4E-02 0 0
CUI: C1836027
Disease: Deafness, Autosomal Recessive 23
Deafness, Autosomal Recessive 23
1 0 1 3.4E-02 0 0
Night Blindness, Congenital Stationary, Autosomal Dominant 1
1 0 1 3.4E-02 0 0