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: C0232874
Disease: Febrile proteinuria
Febrile proteinuria 		1 0 1 0.25 0 0
CUI: C0796028
Disease: ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION
ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION 		1 0 1 0.25 0 0
CUI: C1622439
Disease: Lentiglobus
Lentiglobus 		1 0 1 0.25 0 0
CUI: C1839566
Disease: CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED RECESSIVE, 5 		1 0 1 0.25 0 0
CUI: C1842137
Disease: Nonsyndromic sensorineural hearing loss
Nonsyndromic sensorineural hearing loss 		1 0 1 0.25 0 0
CUI: C2713392
Disease: Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency
Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency 		1 0 1 0.25 0 0
CUI: C4022041
Disease: Hypoammonemia
Hypoammonemia 		1 0 1 0.25 0 0
CUI: C4024743
Disease: Aplasia/Hypoplasia of the optic nerve
Aplasia/Hypoplasia of the optic nerve 		1 0 1 0.25 0 0
CUI: C4024767
Disease: Dense posterior cortical cataract
Dense posterior cortical cataract 		1 0 1 0.25 0 0
CUI: C4305529
Disease: Dent disease type 2
Dent disease type 2 		1 0 1 0.25 0 0
CUI: C4476851
Disease: 5-minute APGAR score of 1
5-minute APGAR score of 1 		1 0 1 0.25 0 0
CUI: C4476857
Disease: 1-minute APGAR score of 0
1-minute APGAR score of 0 		1 0 1 0.25 0 0
CUI: C4706469
Disease: X-linked Charcot-Marie-Tooth disease type 5
X-linked Charcot-Marie-Tooth disease type 5 		1 0 1 0.25 0 0
CUI: C0241760
Disease: Wrist swelling
Wrist swelling 		2 0 1 0.20 0 0
CUI: C0812435
Disease: Chromosome 11p deletion syndrome
Chromosome 11p deletion syndrome 		2 0 1 0.20 0 0
CUI: C1839865
Disease: Bicarbonaturia
Bicarbonaturia 		2 0 1 0.20 0 0
CUI: C1844677
Disease: DEAFNESS, X-LINKED 1 (disorder)
DEAFNESS, X-LINKED 1 (disorder) 		2 0 1 0.20 0 0
CUI: C1854260
Disease: LEBER CONGENITAL AMAUROSIS 6 (disorder)
LEBER CONGENITAL AMAUROSIS 6 (disorder) 		2 0 1 0.20 0 0
CUI: C2673873
Disease: BARDET-BIEDL SYNDROME 13
BARDET-BIEDL SYNDROME 13 		2 0 1 0.20 0 0
CUI: C2713583
Disease: Congenital Tracheobronchomegaly
Congenital Tracheobronchomegaly 		2 0 1 0.20 0 0
CUI: C4023815
Disease: Oligosacchariduria
Oligosacchariduria 		2 0 1 0.20 0 0
CUI: C4024706
Disease: Spinal cord posterior columns myelin loss
Spinal cord posterior columns myelin loss 		2 0 1 0.20 0 0
CUI: C4310705
Disease: JOUBERT SYNDROME 28
JOUBERT SYNDROME 28 		2 0 1 0.20 0 0
CUI: C0948643
Disease: Hyperuricosuria
Hyperuricosuria 		3 0 1 0.17 0 0
CUI: C1845167
Disease: Dent Disease 2
Dent Disease 2 		3 0 1 0.17 0 0