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: C0855197
Disease: Malignant Testicular Germ Cell Tumor
Malignant Testicular Germ Cell Tumor 		0 62 0 0 1 1.0E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 5.6E-02
CUI: C1140680
Disease: Malignant neoplasm of ovary
Malignant neoplasm of ovary 		0 315 0 0 1 2.9E-03
CUI: C1262313
Disease: Invasive Fungal Infections
Invasive Fungal Infections 		0 5 0 0 1 2.5E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 2.7E-02
CUI: C1264195
Disease: Refractory anemia with ringed sideroblasts
Refractory anemia with ringed sideroblasts 		0 3 0 0 2 5.4E-02
CUI: C1333177
Disease: Lymphoproliferative Disorder of the Skin
Lymphoproliferative Disorder of the Skin 		0 4 0 0 1 2.6E-02
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS 		0 37 0 0 2 2.8E-02
CUI: C4082937
Disease: Necrotizing enterocolitis in fetus OR newborn
Necrotizing enterocolitis in fetus OR newborn 		0 26 0 0 1 1.6E-02
CUI: C0007862
Disease: Cervico-Brachial Neuralgia
Cervico-Brachial Neuralgia 		1 0 1 3.8E-02 0 0
CUI: C0085920
Disease: Brachial Neuralgia
Brachial Neuralgia 		1 0 1 3.8E-02 0 0
CUI: C0152072
Disease: Ovale malaria
Ovale malaria 		1 0 1 3.8E-02 0 0
CUI: C0241850
Disease: COORDINATION DEFICIT
COORDINATION DEFICIT 		1 0 1 3.8E-02 0 0
CUI: C0267795
Disease: Subacute hepatic necrosis
Subacute hepatic necrosis 		1 1 1 3.8E-02 1 2.8E-02
CUI: C0271905
Disease: Acquired methemoglobinemia
Acquired methemoglobinemia 		1 0 1 3.8E-02 0 0
CUI: C0272132
Disease: Drug-induced hemolytic anemia
Drug-induced hemolytic anemia 		1 0 1 3.8E-02 0 0
CUI: C0339697
Disease: Congenital color blindness
Congenital color blindness 		1 0 1 3.8E-02 0 0
CUI: C0746365
Disease: malaria relapse
malaria relapse 		1 0 1 3.8E-02 0 0
CUI: C0865236
Disease: Acute intravascular hemolysis
Acute intravascular hemolysis 		1 0 1 3.8E-02 0 0
CUI: C0865274
Disease: High-oxygen-affinity hemoglobin
High-oxygen-affinity hemoglobin 		1 0 1 3.8E-02 0 0
CUI: C1837229
Disease: Muscular Dystrophy, Congenital, Type 1D
Muscular Dystrophy, Congenital, Type 1D 		1 0 1 3.8E-02 0 0
CUI: C1868355
Disease: 6-Phosphogluconolactonase Deficiency
6-Phosphogluconolactonase Deficiency 		1 0 1 3.8E-02 0 0
CUI: C2673517
Disease: PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO
PORPHYRIA CUTANEA TARDA, SUSCEPTIBILITY TO 		1 1 1 3.8E-02 1 2.8E-02
CUI: C2673518
Disease: PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO
PORPHYRIA VARIEGATA, SUSCEPTIBILITY TO 		1 1 1 3.8E-02 1 2.8E-02
CUI: C2673520
Disease: MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding)
MICROVASCULAR COMPLICATIONS OF DIABETES, SUSCEPTIBILITY TO, 7 (finding) 		1 2 1 3.8E-02 2 5.6E-02