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: C0233737
Disease: Circumlocution
Circumlocution
1 0 1 0.20 0 0
POSTERIOR COLUMN ATAXIA WITH RETINITIS PIGMENTOSA
1 0 1 0.20 0 0
CUI: C1842382
Disease: Epilepsy, Benign Neonatal, 3
Epilepsy, Benign Neonatal, 3
1 0 1 0.20 0 0
HYPOMYELINATION AND CONGENITAL CATARACT
1 0 1 0.20 0 0
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 11
1 65 1 0.20 1 1.5E-02
Early infantile epileptic encephalopathy, refractory
1 0 1 0.20 0 0
MENTAL RETARDATION, AUTOSOMAL DOMINANT 31
1 29 1 0.20 1 3.3E-02
Abnormal sensory nerve conduction velocity
1 0 1 0.20 0 0
CUI: C4708498
Disease: PURA syndrome
PURA syndrome
1 0 1 0.20 0 0
NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES
1 0 1 0.20 0 0
CUI: C0265097
Disease: Basilar Artery Stenosis
Basilar Artery Stenosis
2 0 1 0.17 0 0
CUI: C0426908
Disease: Telescoping of limb at hip
Telescoping of limb at hip
2 0 1 0.17 0 0
CUI: C0438434
Disease: Scotoma, Ring
Scotoma, Ring
2 0 1 0.17 0 0
CUI: C0867390
Disease: postoperative stroke
postoperative stroke
2 0 1 0.17 0 0
CUI: C1263853
Disease: Paralytic stroke
Paralytic stroke
2 0 1 0.17 0 0
CUI: C1867923
Disease: Posterior column ataxia
Posterior column ataxia
2 0 1 0.17 0 0
Epilepsy, Familial Mesial Temporal Lobe
2 0 1 0.17 0 0
CUI: C3151685
Disease: Seizures in the newborn, refractory
Seizures in the newborn, refractory
2 0 1 0.17 0 0
CUI: C3203738
Disease: Fowler syndrome
Fowler syndrome
2 0 1 0.17 0 0
CUI: C0018946
Disease: Hematoma, Subdural
Hematoma, Subdural
3 1 1 0.14 1 0.50
CUI: C0085164
Disease: Leukemia, Feline
Leukemia, Feline
3 0 1 0.14 0 0
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTAL DELAY
3 0 1 0.14 0 0
CUI: C0265098
Disease: Basilar artery occlusion
Basilar artery occlusion
4 0 1 0.12 0 0
CUI: C0857345
Disease: Late onset epilepsy
Late onset epilepsy
4 0 1 0.12 0 0
SEIZURES, BENIGN FAMILIAL INFANTILE, 3
4 46 1 0.12 1 2.1E-02