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: C0684324
Disease: Deficiency of phosphoglycerate kinase
Deficiency of phosphoglycerate kinase 		3 6 3 1.00 5 0.56
CUI: C1970848
Disease: Phosphoglycerate Kinase 1 Deficiency
Phosphoglycerate Kinase 1 Deficiency 		3 18 3 1.00 5 0.24
CUI: C1840284
Disease: LEBER CONGENITAL AMAUROSIS 11
LEBER CONGENITAL AMAUROSIS 11 		1 0 1 0.33 0 0
CUI: C4732750
Disease: Decreased hemoglobin concentration
Decreased hemoglobin concentration 		1 0 1 0.33 0 0
CUI: C1845359
Disease: Spinal Muscular Atrophy, Distal, X-Linked 3
Spinal Muscular Atrophy, Distal, X-Linked 3 		2 0 1 0.25 0 0
CUI: C1842475
Disease: Retinitis Pigmentosa 7
Retinitis Pigmentosa 7 		7 0 1 0.11 0 0
CUI: C1519665
Disease: Tumor-Associated Process
Tumor-Associated Process 		8 0 1 1.0E-01 0 0
CUI: C1845155
Disease: Exercise-induced myoglobinuria
Exercise-induced myoglobinuria 		8 0 1 1.0E-01 0 0
CUI: C1855578
Disease: Exercise-induced muscle cramps
Exercise-induced muscle cramps 		8 0 1 1.0E-01 0 0
CUI: C3540662
Disease: Congenital Amaurosis of Retinal Origin
Congenital Amaurosis of Retinal Origin 		8 0 1 1.0E-01 0 0
CUI: C1844830
Disease: CLEFT PALATE, X-LINKED
CLEFT PALATE, X-LINKED 		9 0 1 9.1E-02 0 0
CUI: C0393808
Disease: Charcot-Marie-Tooth disease, X-linked, 1
Charcot-Marie-Tooth disease, X-linked, 1 		10 0 1 8.3E-02 0 0
CUI: C4021570
Disease: Undetectable light- and dark-adapted electroretinogram
Undetectable light- and dark-adapted electroretinogram 		11 0 1 7.7E-02 0 0
CUI: C0240997
Disease: Decreased serum ceruloplasmin
Decreased serum ceruloplasmin 		12 0 1 7.1E-02 0 0
CUI: C0948168
Disease: Bone marrow toxicity
Bone marrow toxicity 		13 0 1 6.7E-02 0 0
CUI: C1855514
Disease: Severe failure to thrive
Severe failure to thrive 		14 0 1 6.2E-02 0 0
CUI: C1839130
Disease: Dystonia 3, Torsion, X-Linked
Dystonia 3, Torsion, X-Linked 		15 0 1 5.9E-02 0 0
CUI: C4023722
Disease: Abnormality of hair texture
Abnormality of hair texture 		15 0 1 5.9E-02 0 0
CUI: C0005754
Disease: Congenital blindness
Congenital blindness 		16 0 1 5.6E-02 0 0
CUI: C0027080
Disease: Myoglobinuria
Myoglobinuria 		17 0 1 5.3E-02 0 0
CUI: C1855580
Disease: Exercise-induced muscle fatigue
Exercise-induced muscle fatigue 		18 0 1 5.0E-02 0 0
CUI: C0022716
Disease: Menkes Kinky Hair Syndrome
Menkes Kinky Hair Syndrome 		20 0 1 4.5E-02 0 0
CUI: C0271682
Disease: Mixed sensory-motor polyneuropathy
Mixed sensory-motor polyneuropathy 		20 0 1 4.5E-02 0 0
CUI: C0162359
Disease: Christ-Siemens-Touraine syndrome
Christ-Siemens-Touraine syndrome 		45 0 2 4.3E-02 0 0
CUI: C0268353
Disease: Cutis laxa, x-linked
Cutis laxa, x-linked 		22 0 1 4.2E-02 0 0