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: C0162292
Disease: External Ophthalmoplegia
External Ophthalmoplegia 		41 0 1 9.7E-04 0 0
CUI: C0231921
Disease: Pulmonary function
Pulmonary function 		41 0 1 9.7E-04 0 0
CUI: C0241816
Disease: Global brain atrophy
Global brain atrophy 		41 0 1 9.7E-04 0 0
CUI: C0270834
Disease: Complex partial seizure with impairment of consciousness
Complex partial seizure with impairment of consciousness 		41 0 1 9.7E-04 0 0
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		41 0 1 9.7E-04 0 0
CUI: C0581354
Disease: Recurrent sinusitis
Recurrent sinusitis 		41 0 1 9.7E-04 0 0
CUI: C3160731
Disease: Pulmonary function (finding)
Pulmonary function (finding) 		41 0 1 9.7E-04 0 0
CUI: C0085606
Disease: Urgency of micturition
Urgency of micturition 		40 0 1 9.7E-04 0 0
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY 		40 0 1 9.7E-04 0 0
CUI: C1956147
Disease: Microlissencephaly
Microlissencephaly 		40 0 1 9.7E-04 0 0
CUI: C4021815
Disease: Abnormal palate morphology
Abnormal palate morphology 		40 0 1 9.7E-04 0 0
CUI: C4024780
Disease: Almond-shaped palpebral fissure
Almond-shaped palpebral fissure 		40 0 1 9.7E-04 0 0
CUI: C1847515
Disease: Paroxysmal involuntary eye movements
Paroxysmal involuntary eye movements 		39 0 1 9.7E-04 0 0
CUI: C2749675
Disease: Cortical gyral simplification
Cortical gyral simplification 		39 0 1 9.7E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 9.7E-04 0 0
CUI: C1838681
Disease: Rapidly progressive
Rapidly progressive 		38 0 1 9.8E-04 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration 		37 0 1 9.8E-04 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 0 1 9.8E-04 0 0
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius 		37 0 1 9.8E-04 0 0
CUI: C1837732
Disease: Thickened helices
Thickened helices 		37 0 1 9.8E-04 0 0
CUI: C0752122
Disease: Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 4 		36 0 1 9.8E-04 0 0
CUI: C1305849
Disease: Diastolic blood pressure measurement
Diastolic blood pressure measurement 		35 0 1 9.8E-04 0 0
CUI: C1832348
Disease: Slow-growing hair
Slow-growing hair 		35 0 1 9.8E-04 0 0
CUI: C3853041
Disease: Severe Congenital Microcephaly
Severe Congenital Microcephaly 		35 0 1 9.8E-04 0 0
CUI: C0454651
Disease: Specific language impairment
Specific language impairment 		34 0 1 9.8E-04 0 0