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: C4025797
Disease: Abnormality of prenatal development or birth
Abnormality of prenatal development or birth 		23 0 1 4.3E-02 0 0
CUI: C0241267
Disease: Absence of subcutaneous fat
Absence of subcutaneous fat 		11 0 1 9.1E-02 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor 		95 0 1 1.1E-02 0 0
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		685 0 1 1.5E-03 0 0
CUI: C0002871
Disease: Anemia
Anemia 		847 0 1 1.2E-03 0 0
CUI: C1859077
Disease: Aplasia/Hypoplasia of the nails
Aplasia/Hypoplasia of the nails 		14 0 1 7.1E-02 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism 		148 0 1 6.8E-03 0 0
CUI: C1843496
Disease: Bilateral microphthalmos
Bilateral microphthalmos 		35 0 1 2.9E-02 0 0
CUI: C1837758
Disease: Bird-like facies
Bird-like facies 		12 0 1 8.3E-02 0 0
CUI: C0263490
Disease: Brittle hair
Brittle hair 		45 0 1 2.2E-02 0 0
CUI: C0856863
Disease: Broad-based gait
Broad-based gait 		75 0 1 1.3E-02 0 0
CUI: C0006266
Disease: Bronchospasm
Bronchospasm 		29 0 1 3.4E-02 0 0
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		6243 0 1 1.6E-04 0 0
CUI: C0878544
Disease: Cardiomyopathies
Cardiomyopathies 		925 0 1 1.1E-03 0 0
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		226 0 1 4.4E-03 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		271 0 1 3.7E-03 0 0
CUI: C1854885
Disease: Cerebral dysmyelination
Cerebral dysmyelination 		17 0 1 5.9E-02 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		410 0 1 2.4E-03 0 0
CUI: C0401151
Disease: Chronic diarrhea
Chronic diarrhea 		62 0 1 1.6E-02 0 0
CUI: C0399526
Disease: Class III malocclusion
Class III malocclusion 		181 0 1 5.5E-03 0 0
CUI: C0009080
Disease: Clubbed Fingers
Clubbed Fingers 		88 0 1 1.1E-02 0 0
CUI: C0149651
Disease: Clubbing
Clubbing 		32 0 1 3.1E-02 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features 		194 0 1 5.2E-03 0 0
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		417 0 1 2.4E-03 0 0
CUI: C4024892
Disease: Congenital exfoliative erythroderma
Congenital exfoliative erythroderma 		6 0 1 0.17 0 0