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: C0220624
Disease: Adult Brain Neoplasm
Adult Brain Neoplasm 		15 0 2 6.9E-02 0 0
CUI: C0334619
Disease: HODGKIN'S AND NON-HODGKIN'S LYMPHOMA
HODGKIN'S AND NON-HODGKIN'S LYMPHOMA 		17 0 2 6.5E-02 0 0
CUI: C1827820
Disease: Fast acetylator due to N-acetyltransferase enzyme variant
Fast acetylator due to N-acetyltransferase enzyme variant 		17 0 2 6.5E-02 0 0
CUI: C0004698
Disease: Balkan Nephropathy
Balkan Nephropathy 		34 0 3 6.4E-02 0 0
CUI: C0338437
Disease: Neurocysticercosis
Neurocysticercosis 		34 0 3 6.4E-02 0 0
CUI: C0751038
Disease: Cockayne Syndrome, Type II
Cockayne Syndrome, Type II 		34 0 3 6.4E-02 0 0
CUI: C0016978
Disease: gallbladder neoplasm
gallbladder neoplasm 		51 0 4 6.3E-02 0 0
CUI: C0085692
Disease: Hemorrhagic cystitis
Hemorrhagic cystitis 		18 0 2 6.2E-02 0 0
CUI: C0154298
Disease: Acute posthaemorrhagic anaemia
Acute posthaemorrhagic anaemia 		1 0 1 6.2E-02 0 0
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I 		18 0 2 6.2E-02 0 0
CUI: C0279822
Disease: recurrent pheochromocytoma
recurrent pheochromocytoma 		1 0 1 6.2E-02 0 0
CUI: C0410652
Disease: Cervical spine instability
Cervical spine instability 		1 0 1 6.2E-02 0 0
CUI: C0856823
Disease: Undifferentiated type acute leukemia
Undifferentiated type acute leukemia 		1 0 1 6.2E-02 0 0
CUI: C0862039
Disease: Precursor B-lymphoblastic lymphoma stage II
Precursor B-lymphoblastic lymphoma stage II 		1 0 1 6.2E-02 0 0
CUI: C0948824
Disease: Anemia due to blood loss
Anemia due to blood loss 		1 0 1 6.2E-02 0 0
CUI: C0969687
Disease: Autosomal Chromosome Disorders
Autosomal Chromosome Disorders 		1 0 1 6.2E-02 0 0
CUI: C1336727
Disease: Testicular Sarcoma
Testicular Sarcoma 		1 0 1 6.2E-02 0 0
CUI: C1517445
Disease: Ganglioneuroblastoma, Nodular
Ganglioneuroblastoma, Nodular 		1 0 1 6.2E-02 0 0
CUI: C1851057
Disease: Normal motor development
Normal motor development 		1 0 1 6.2E-02 0 0
CUI: C1853100
Disease: CEREBROOCULOFACIOSKELETAL SYNDROME 4
CEREBROOCULOFACIOSKELETAL SYNDROME 4 		1 0 1 6.2E-02 0 0
CUI: C1969649
Disease: KALA-AZAR, SUSCEPTIBILITY TO, 2
KALA-AZAR, SUSCEPTIBILITY TO, 2 		1 0 1 6.2E-02 0 0
CUI: C2673187
Disease: Erythrocytosis, Familial, 4
Erythrocytosis, Familial, 4 		1 0 1 6.2E-02 0 0
CUI: C4014476
Disease: MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10
MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 10 		1 0 1 6.2E-02 0 0
CUI: C4015156
Disease: MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE
MICROCEPHALY 12, PRIMARY, AUTOSOMAL RECESSIVE 		1 0 1 6.2E-02 0 0
CUI: C4025295
Disease: Elbow hypertrichosis
Elbow hypertrichosis 		1 0 1 6.2E-02 0 0