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: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 0.20 0 0
CUI: C0543837
Disease: Respiratory distress syndrome, children
Respiratory distress syndrome, children 		1 0 1 0.20 0 0
CUI: C1955871
Disease: Cobblestone Complex
Cobblestone Complex 		1 0 1 0.20 0 0
CUI: C3806616
Disease: Macular hypopigmented whorls, streaks, and patches
Macular hypopigmented whorls, streaks, and patches 		1 0 1 0.20 0 0
CUI: C3810405
Disease: POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE
POLYMICROGYRIA, BILATERAL PERISYLVIAN, AUTOSOMAL RECESSIVE 		1 0 1 0.20 0 0
CUI: C3888212
Disease: SECKEL SYNDROME 4
SECKEL SYNDROME 4 		1 0 1 0.20 0 0
CUI: C4021030
Disease: Type III lissencephaly
Type III lissencephaly 		1 2 1 0.20 2 0.67
CUI: C4023074
Disease: EEG with parietal focal spikes
EEG with parietal focal spikes 		1 0 1 0.20 0 0
CUI: C4024854
Disease: Irregular hyperpigmentation of back
Irregular hyperpigmentation of back 		1 0 1 0.20 0 0
CUI: C4225259
Disease: SMITH-KINGSMORE SYNDROME
SMITH-KINGSMORE SYNDROME 		1 0 1 0.20 0 0
CUI: C4476709
Disease: Delayed ability to stand
Delayed ability to stand 		1 0 1 0.20 0 0
CUI: C4476941
Disease: Impaired toileting ability
Impaired toileting ability 		1 0 1 0.20 0 0
CUI: C4479673
Disease: FOCAL CORTICAL DYSPLASIA, TYPE II, SOMATIC
FOCAL CORTICAL DYSPLASIA, TYPE II, SOMATIC 		1 0 1 0.20 0 0
CUI: C4551756
Disease: Waldenstrom's macroglobulinaemia refractory
Waldenstrom's macroglobulinaemia refractory 		1 0 1 0.20 0 0
CUI: C4724572
Disease: Obstructive apnea
Obstructive apnea 		1 0 1 0.20 0 0
CUI: C0013691
Disease: Chylous effusion
Chylous effusion 		2 0 1 0.17 0 0
CUI: C0031880
Disease: Obesity Hypoventilation Syndrome
Obesity Hypoventilation Syndrome 		2 0 1 0.17 0 0
CUI: C0858259
Disease: Nasal discomfort
Nasal discomfort 		2 0 1 0.17 0 0
CUI: C1260966
Disease: Central odontogenic fibroma
Central odontogenic fibroma 		2 0 1 0.17 0 0
CUI: C1835764
Disease: Vertebral arch anomaly
Vertebral arch anomaly 		2 0 1 0.17 0 0
CUI: C1866245
Disease: Hyperpigmented streaks
Hyperpigmented streaks 		2 0 1 0.17 0 0
CUI: C3150931
Disease: Steep acetabular roof
Steep acetabular roof 		2 0 1 0.17 0 0
CUI: C3151187
Disease: SECKEL SYNDROME 5
SECKEL SYNDROME 5 		2 0 1 0.17 0 0
CUI: C4022871
Disease: Extra-axial cerebrospinal fluid accumulation
Extra-axial cerebrospinal fluid accumulation 		2 0 1 0.17 0 0
CUI: C4023073
Disease: EEG with temporal focal spikes
EEG with temporal focal spikes 		2 0 1 0.17 0 0