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: C1836217
Disease: Tukel syndrome
Tukel syndrome
2 0 2 1.00 0 0
CUI: C1846911
Disease: Compensatory chin elevation
Compensatory chin elevation
2 0 2 1.00 0 0
Levator palpebrae superioris atrophy
2 0 2 1.00 0 0
CUI: C1851108
Disease: Superior rectus atrophy
Superior rectus atrophy
2 0 2 1.00 0 0
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B (disorder)
2 0 2 1.00 0 0
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 2
3 0 2 0.67 0 0
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3A, WITH OR WITHOUT EXTRAOCULAR INVOLVEMENT
3 0 2 0.67 0 0
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 5
3 0 2 0.67 0 0
CUI: C0234175
Disease: Palmar reflex
Palmar reflex
1 0 1 0.50 0 0
CUI: C0234435
Disease: Syncope, Tussive
Syncope, Tussive
1 0 1 0.50 0 0
CUI: C0339624
Disease: Secondary Esotropia
Secondary Esotropia
1 0 1 0.50 0 0
CUI: C1276000
Disease: Sensory exotropia
Sensory exotropia
1 0 1 0.50 0 0
CUI: C1851087
Disease: Agenesis of the anterior commissure
Agenesis of the anterior commissure
1 0 1 0.50 0 0
Fibrosis Of Extraocular Muscles, Congenital, 1
4 0 2 0.50 0 0
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1
1 0 1 0.50 0 0
Nonprogressive restrictive external ophthalmoplegia
1 0 1 0.50 0 0
CUI: C0152221
Disease: Paralytic strabismus
Paralytic strabismus
2 0 1 0.33 0 0
CUI: C0266521
Disease: Marcus Gunn phenomenon
Marcus Gunn phenomenon
2 0 1 0.33 0 0
Abnormal best corrected visual acuity test
2 0 1 0.33 0 0
Restrictive external ophthalmoplegia
3 0 1 0.25 0 0
CUI: C2062713
Disease: Progressive ophthalmoplegia
Progressive ophthalmoplegia
3 0 1 0.25 0 0
CUI: C4476710
Disease: Delayed ability to sit
Delayed ability to sit
3 0 1 0.25 0 0
CUI: C0028850
Disease: Ocular Motility Disorders
Ocular Motility Disorders
9 0 2 0.22 0 0
Secondary malignant neoplasm of rectum
4 0 1 0.20 0 0
CUI: C0861772
Disease: Stage IV Rectal Carcinoma
Stage IV Rectal Carcinoma
4 0 1 0.20 0 0