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: C0020575
Disease: Hypertropia
Hypertropia 		1 0 1 7.7E-02 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 7.7E-02 0 0
CUI: C0234175
Disease: Palmar reflex
Palmar reflex 		1 0 1 7.7E-02 0 0
CUI: C0234435
Disease: Syncope, Tussive
Syncope, Tussive 		1 1 1 7.7E-02 1 0.25
CUI: C0276839
Disease: Infection by Cytauxzoon
Infection by Cytauxzoon 		1 0 1 7.7E-02 0 0
CUI: C0339624
Disease: Secondary Esotropia
Secondary Esotropia 		1 0 1 7.7E-02 0 0
CUI: C0339648
Disease: Strabismus fixus
Strabismus fixus 		1 0 1 7.7E-02 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 7.7E-02 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 7.7E-02 0 0
CUI: C1276000
Disease: Sensory exotropia
Sensory exotropia 		1 0 1 7.7E-02 0 0
CUI: C1839580
Disease: Nystagmus 1, congenital, X- linked
Nystagmus 1, congenital, X- linked 		1 0 1 7.7E-02 0 0
CUI: C1840365
Disease: King Denborough syndrome
King Denborough syndrome 		1 0 1 7.7E-02 0 0
CUI: C1851087
Disease: Agenesis of the anterior commissure
Agenesis of the anterior commissure 		1 0 1 7.7E-02 0 0
CUI: C1861753
Disease: Multiminicore Disease, Moderate, with Hand Involvement
Multiminicore Disease, Moderate, with Hand Involvement 		1 0 1 7.7E-02 0 0
CUI: C2083352
Disease: Rectus femoris muscle atrophy
Rectus femoris muscle atrophy 		1 0 1 7.7E-02 0 0
CUI: C2315667
Disease: Fetal microcephaly
Fetal microcephaly 		1 0 1 7.7E-02 0 0
CUI: C2674259
Disease: NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder)
NEUROMUSCULAR DISEASE, CONGENITAL, WITH UNIFORM TYPE 1 FIBER (disorder) 		1 0 1 7.7E-02 0 0
CUI: C2677687
Disease: Mildly reduced visual acuity
Mildly reduced visual acuity 		1 0 1 7.7E-02 0 0
CUI: C2752061
Disease: Cerebral Palsy, Spastic Quadriplegic, 2
Cerebral Palsy, Spastic Quadriplegic, 2 		1 0 1 7.7E-02 0 0
CUI: C2930980
Disease: Malignant hyperthermia susceptibility type 1
Malignant hyperthermia susceptibility type 1 		1 0 1 7.7E-02 0 0
CUI: C2931644
Disease: O'Donnell Pappas syndrome
O'Donnell Pappas syndrome 		1 0 1 7.7E-02 0 0
CUI: C3552236
Disease: CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 7 		1 14 1 7.7E-02 1 5.9E-02
CUI: C3640024
Disease: Unilateral microphthalmos
Unilateral microphthalmos 		1 0 1 7.7E-02 0 0
CUI: C3805349
Disease: CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY
CATARACTS, CONGENITAL, WITH LATE-ONSET CORNEAL DYSTROPHY 		1 0 1 7.7E-02 0 0
CUI: C3808397
Disease: CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1
CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 1 		1 10 1 7.7E-02 1 7.7E-02