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: C1283397
Disease: Deficiency of acetylcholinesterase
Deficiency of acetylcholinesterase 		5 0 2 0.22 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 0.17 0 0
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 0.17 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 0.17 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 0.17 0 0
CUI: C0340074
Disease: Postoperative atelectasis
Postoperative atelectasis 		1 0 1 0.17 0 0
CUI: C0746365
Disease: malaria relapse
malaria relapse 		1 0 1 0.17 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple 		1 0 1 0.17 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p 		1 0 1 0.17 0 0
CUI: C0865236
Disease: Acute intravascular hemolysis
Acute intravascular hemolysis 		1 0 1 0.17 0 0
CUI: C1263777
Disease: Neoplasm of body of uterus
Neoplasm of body of uterus 		1 0 1 0.17 0 0
CUI: C1695985
Disease: Lewis-Sumner syndrome
Lewis-Sumner syndrome 		1 0 1 0.17 0 0
CUI: C1861669
Disease: Charcot-Marie-Tooth disease and deafness
Charcot-Marie-Tooth disease and deafness 		1 0 1 0.17 0 0
CUI: C1868355
Disease: 6-Phosphogluconolactonase Deficiency
6-Phosphogluconolactonase Deficiency 		1 0 1 0.17 0 0
CUI: C2931686
Disease: Charcot-Marie-Tooth disease, Type 1E
Charcot-Marie-Tooth disease, Type 1E 		1 0 1 0.17 0 0
CUI: C3495591
Disease: Charcot-Marie-Tooth Disease, Demyelinating, Type 1e
Charcot-Marie-Tooth Disease, Demyelinating, Type 1e 		1 0 1 0.17 0 0
CUI: C4016522
Disease: G6PD TOMAH PHENOTYPE
G6PD TOMAH PHENOTYPE 		1 0 1 0.17 0 0
CUI: C4016716
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, AUTOSOMAL RECESSIVE
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, AUTOSOMAL RECESSIVE 		1 0 1 0.17 0 0
CUI: C4016717
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, WITH FOCALLY FOLDED MYELIN SHEATHS
CHARCOT-MARIE-TOOTH DISEASE, TYPE 1A, WITH FOCALLY FOLDED MYELIN SHEATHS 		1 0 1 0.17 0 0
CUI: C4020904
Disease: Myelin tomacula
Myelin tomacula 		1 0 1 0.17 0 0
CUI: C4023690
Disease: Spontaneous pain sensation
Spontaneous pain sensation 		1 0 1 0.17 0 0
CUI: C4024933
Disease: Acute demyelinating polyneuropathy
Acute demyelinating polyneuropathy 		1 0 1 0.17 0 0
CUI: C4302087
Disease: Silent cerebral infarct
Silent cerebral infarct 		1 0 1 0.17 0 0
CUI: C4317046
Disease: Hematological abnormality
Hematological abnormality 		1 0 1 0.17 0 0
CUI: C4755276
Disease: Primary CD59 deficiency
Primary CD59 deficiency 		1 0 1 0.17 0 0