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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 2.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.6E-02
CUI: C0233689
Disease: Delusion of infidelity
Delusion of infidelity 		0 1 0 0 1 2.6E-02
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 2.6E-02
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome 		0 1 0 0 1 2.6E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.6E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.5E-02
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0 10 0 0 1 2.1E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.6E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 5.1E-02
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 1.5E-03 0 0
CUI: C4049938
Disease: Physical Activity Measurement
Physical Activity Measurement 		160 0 1 1.5E-03 0 0
CUI: C0037773
Disease: Spastic Paraplegia, Hereditary
Spastic Paraplegia, Hereditary 		123 0 1 1.6E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		104 0 1 1.6E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 1.6E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc 		98 0 1 1.7E-03 0 0
CUI: C0005893
Disease: Body mass index procedure
Body mass index procedure 		88 0 1 1.7E-03 0 0
CUI: C0578022
Disease: Finding of body mass index
Finding of body mass index 		88 0 1 1.7E-03 0 0
CUI: C0752166
Disease: Bardet-Biedl Syndrome
Bardet-Biedl Syndrome 		86 0 1 1.7E-03 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis 		85 0 1 1.7E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.7E-03 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia 		77 0 1 1.7E-03 0 0
CUI: C0424551
Disease: Impaired exercise tolerance
Impaired exercise tolerance 		76 0 1 1.7E-03 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 1.7E-03 0 0
CUI: C0426848
Disease: Sacral dimple
Sacral dimple 		69 0 1 1.7E-03 0 0