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: C0234458
Disease: Dream disorder
Dream disorder 		1 0 1 1.0E-01 0 0
CUI: C0339882
Disease: Laryngeal amyloidosis
Laryngeal amyloidosis 		1 0 1 1.0E-01 0 0
CUI: C0346064
Disease: Cutaneous leiomyoma
Cutaneous leiomyoma 		1 0 1 1.0E-01 0 0
CUI: C0346067
Disease: Cutaneous Leiomyosarcoma
Cutaneous Leiomyosarcoma 		1 0 1 1.0E-01 0 0
CUI: C0458118
Disease: Total body pain syndrome
Total body pain syndrome 		1 0 1 1.0E-01 0 0
CUI: C0751544
Disease: Tangier Disease Neuropathy
Tangier Disease Neuropathy 		1 0 1 1.0E-01 0 0
CUI: C0862953
Disease: Cholangiocarcinoma non-resectable
Cholangiocarcinoma non-resectable 		1 0 1 1.0E-01 0 0
CUI: C1274408
Disease: Chronic plaque-like oral candidiasis
Chronic plaque-like oral candidiasis 		1 0 1 1.0E-01 0 0
CUI: C1306229
Disease: Dyschromatosis universalis
Dyschromatosis universalis 		1 0 1 1.0E-01 0 0
CUI: C1836705
Disease: Pseudohyperkalemia, Familial, 2, due to Red Cell Leak
Pseudohyperkalemia, Familial, 2, due to Red Cell Leak 		1 0 1 1.0E-01 0 0
CUI: C1850644
Disease: Anterior bowing of long bones
Anterior bowing of long bones 		1 0 1 1.0E-01 0 0
CUI: C1853903
Disease: Decreased fumarate hydratase activity
Decreased fumarate hydratase activity 		1 0 1 1.0E-01 0 0
CUI: C2711472
Disease: Infection by Trypanosoma brucei brucei
Infection by Trypanosoma brucei brucei 		1 0 1 1.0E-01 0 0
CUI: C2880381
Disease: Arcus senilis, bilateral
Arcus senilis, bilateral 		1 0 1 1.0E-01 0 0
CUI: C3549860
Disease: Uterine leiomyosarcoma (less common)
Uterine leiomyosarcoma (less common) 		1 0 1 1.0E-01 0 0
CUI: C3549861
Disease: Cutaneous leiomyosarcoma (less common)
Cutaneous leiomyosarcoma (less common) 		1 0 1 1.0E-01 0 0
CUI: C3549862
Disease: Renal cell carcinoma, solitary papillary type 2 (about 20% of patients)
Renal cell carcinoma, solitary papillary type 2 (about 20% of patients) 		1 0 1 1.0E-01 0 0
CUI: C3809394
Disease: DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3
DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3 		1 0 1 1.0E-01 0 0
CUI: C4015830
Disease: APOLIPOPROTEIN A-I (MILANO) PHENOTYPE
APOLIPOPROTEIN A-I (MILANO) PHENOTYPE 		1 0 1 1.0E-01 0 0
CUI: C4015832
Disease: APOLIPOPROTEIN A-I (MUNSTER4) PHENOTYPE
APOLIPOPROTEIN A-I (MUNSTER4) PHENOTYPE 		1 0 1 1.0E-01 0 0
CUI: C4015833
Disease: APOLIPOPROTEIN A-I (GIESSEN) PHENOTYPE
APOLIPOPROTEIN A-I (GIESSEN) PHENOTYPE 		1 0 1 1.0E-01 0 0
CUI: C4016640
Disease: TANGIER DISEASE, VARIANT
TANGIER DISEASE, VARIANT 		1 0 1 1.0E-01 0 0
CUI: C4021969
Disease: Abnormally straight spine
Abnormally straight spine 		1 0 1 1.0E-01 0 0
CUI: C4025034
Disease: Abnormality of femoral epiphysis
Abnormality of femoral epiphysis 		1 0 1 1.0E-01 0 0
CUI: C4087475
Disease: Reed syndrome
Reed syndrome 		1 0 1 1.0E-01 0 0