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: C3806616
Disease: Macular hypopigmented whorls, streaks, and patches
Macular hypopigmented whorls, streaks, and patches 		1 0 1 0.11 0 0
CUI: C4016396
Disease: LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB
LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB 		1 0 1 0.11 0 0
CUI: C4023165
Disease: Abnormality of skeletal morphology
Abnormality of skeletal morphology 		1 0 1 0.11 0 0
CUI: C4024854
Disease: Irregular hyperpigmentation of back
Irregular hyperpigmentation of back 		1 0 1 0.11 0 0
CUI: C4225259
Disease: SMITH-KINGSMORE SYNDROME
SMITH-KINGSMORE SYNDROME 		1 0 1 0.11 0 0
CUI: C4228779
Disease: Increased susceptibility to malignancy
Increased susceptibility to malignancy 		1 0 1 0.11 0 0
CUI: C4287832
Disease: Metastatic Malignant Solid Neoplasm
Metastatic Malignant Solid Neoplasm 		1 0 1 0.11 0 0
CUI: C4288091
Disease: Tubulocystic renal cell carcinoma
Tubulocystic renal cell carcinoma 		1 0 1 0.11 0 0
CUI: C4476709
Disease: Delayed ability to stand
Delayed ability to stand 		1 0 1 0.11 0 0
CUI: C4479673
Disease: FOCAL CORTICAL DYSPLASIA, TYPE II, SOMATIC
FOCAL CORTICAL DYSPLASIA, TYPE II, SOMATIC 		1 0 1 0.11 0 0
CUI: C4525220
Disease: Feline Fibrosarcoma
Feline Fibrosarcoma 		1 0 1 0.11 0 0
CUI: C4539857
Disease: CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME
CONGENITAL HEART DEFECTS AND SKELETAL MALFORMATIONS SYNDROME 		1 0 1 0.11 0 0
CUI: C4551756
Disease: Waldenstrom's macroglobulinaemia refractory
Waldenstrom's macroglobulinaemia refractory 		1 0 1 0.11 0 0
CUI: C4751597
Disease: Fatal post-viral neurodegenerative disorder
Fatal post-viral neurodegenerative disorder 		1 0 1 0.11 0 0
CUI: C0023472
Disease: Leukemia, Myeloid, Accelerated Phase
Leukemia, Myeloid, Accelerated Phase 		12 0 2 0.11 0 0
CUI: C0702266
Disease: Basophilia
Basophilia 		12 0 2 0.11 0 0
CUI: C1327920
Disease: Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive
Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive 		12 0 2 0.11 0 0
CUI: C4049328
Disease: Renal medullary carcinoma
Renal medullary carcinoma 		12 0 2 0.11 0 0
CUI: C0013691
Disease: Chylous effusion
Chylous effusion 		2 0 1 1.0E-01 0 0
CUI: C0085594
Disease: Fever with chills
Fever with chills 		2 0 1 1.0E-01 0 0
CUI: C0264988
Disease: Periarteritis
Periarteritis 		2 0 1 1.0E-01 0 0
CUI: C0272199
Disease: Familial Hemophagocytic Lymphocytosis
Familial Hemophagocytic Lymphocytosis 		35 6 4 1.0E-01 2 6.9E-02
CUI: C0278785
Disease: Recurrent Adult Acute Lymphoblastic Leukemia
Recurrent Adult Acute Lymphoblastic Leukemia 		2 0 1 1.0E-01 0 0
CUI: C0543478
Disease: Residual Tumor
Residual Tumor 		2 0 1 1.0E-01 0 0
CUI: C0851881
Disease: Enterococcal infection
Enterococcal infection 		2 0 1 1.0E-01 0 0