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: C2677682
Disease: Rett Syndrome, Zappella Variant
Rett Syndrome, Zappella Variant 		1 0 1 0.17 0 0
CUI: C2749007
Disease: Chromosome Xq28 Duplication Syndrome
Chromosome Xq28 Duplication Syndrome 		1 0 1 0.17 0 0
CUI: C2749861
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY)
MITOCHONDRIAL DNA DEPLETION SYNDROME 8A (ENCEPHALOMYOPATHIC TYPE WITH RENAL TUBULOPATHY) 		1 0 1 0.17 0 0
CUI: C2751319
Disease: Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5
Progressive External Ophthalmoplegia With Mitochondrial Dna Deletions, Autosomal Dominant, 5 		1 0 1 0.17 0 0
CUI: C2931847
Disease: Type I familial incomplete male pseudohermaphroditism
Type I familial incomplete male pseudohermaphroditism 		1 0 1 0.17 0 0
CUI: C3150172
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 8B (MNGIE TYPE) 		1 0 1 0.17 0 0
CUI: C3713418
Disease: Ppm-X Syndrome
Ppm-X Syndrome 		1 0 1 0.17 0 0
CUI: C3714043
Disease: Trisomy Xq28
Trisomy Xq28 		1 0 1 0.17 0 0
CUI: C4022860
Disease: Maternal anticardiolipin antibody positive
Maternal anticardiolipin antibody positive 		1 0 1 0.17 0 0
CUI: C4025796
Disease: Abnormality of the fingertips
Abnormality of the fingertips 		1 0 1 0.17 0 0
CUI: C4303787
Disease: Ehlers-Danlos syndrome musculocontractural type
Ehlers-Danlos syndrome musculocontractural type 		1 0 1 0.17 0 0
CUI: C0233778
Disease: Synesthesia
Synesthesia 		2 0 1 0.14 0 0
CUI: C0342708
Disease: Gamma aminobutyric acid transaminase deficiency
Gamma aminobutyric acid transaminase deficiency 		2 0 1 0.14 0 0
CUI: C0751355
Disease: Polymyoclonus
Polymyoclonus 		2 0 1 0.14 0 0
CUI: C1833136
Disease: Marden Walker like syndrome
Marden Walker like syndrome 		2 0 1 0.14 0 0
CUI: C1843228
Disease: Hypotrophy of the small hand muscles
Hypotrophy of the small hand muscles 		2 0 1 0.14 0 0
CUI: C1848586
Disease: Visceral myopathy familial external ophthalmoplegia
Visceral myopathy familial external ophthalmoplegia 		2 0 1 0.14 0 0
CUI: C1866294
Disease: EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1
EHLERS-DANLOS SYNDROME, MUSCULOCONTRACTURAL TYPE 1 		2 0 1 0.14 0 0
CUI: C2931713
Disease: Chromosome 17 deletion
Chromosome 17 deletion 		2 0 1 0.14 0 0
CUI: C3683846
Disease: Chromosome 17p Deletion Syndrome
Chromosome 17p Deletion Syndrome 		2 0 1 0.14 0 0
CUI: C4022750
Disease: Thin fingernail
Thin fingernail 		2 0 1 0.14 0 0
CUI: C4023486
Disease: Focal EEG discharges with secondary generalization
Focal EEG discharges with secondary generalization 		2 0 1 0.14 0 0
CUI: C4023523
Disease: Bilateral fetal pyelectasis
Bilateral fetal pyelectasis 		2 0 1 0.14 0 0
CUI: C4025716
Disease: Abnormality of the duodenum
Abnormality of the duodenum 		2 0 1 0.14 0 0
CUI: C4274731
Disease: Jeavons syndrome
Jeavons syndrome 		2 0 1 0.14 0 0