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: C4531035
Disease: Abnormal pulmonary valve cusp morphology
Abnormal pulmonary valve cusp morphology 		2 0 2 0.33 0 0
CUI: C0426636
Disease: Urgent desire for stool
Urgent desire for stool 		3 0 2 0.29 0 0
CUI: C4022606
Disease: Lack of bowel sounds
Lack of bowel sounds 		3 0 2 0.29 0 0
CUI: C4025812
Disease: Dermatological manifestations of systemic disorders
Dermatological manifestations of systemic disorders 		3 0 2 0.29 0 0
CUI: C4072942
Disease: Atypical pulmonary carcinoid tumor
Atypical pulmonary carcinoid tumor 		3 0 2 0.29 0 0
CUI: C0858684
Disease: Facial telangiectasia
Facial telangiectasia 		6 0 2 0.20 0 0
CUI: C0475802
Disease: Perinatal anoxic-ischemic brain injury
Perinatal anoxic-ischemic brain injury 		7 0 2 0.18 0 0
CUI: C0036219
Disease: Sarcoma, Jensen
Sarcoma, Jensen 		1 0 1 0.17 0 0
CUI: C0085307
Disease: Embolism and Thrombosis
Embolism and Thrombosis 		1 0 1 0.17 0 0
CUI: C0152497
Disease: Food poisoning caused by Vibrio parahaemolyticus
Food poisoning caused by Vibrio parahaemolyticus 		1 0 1 0.17 0 0
CUI: C0231618
Disease: Corkscrewing
Corkscrewing 		1 0 1 0.17 0 0
CUI: C0238408
Disease: Hematoma of rectus sheath
Hematoma of rectus sheath 		1 0 1 0.17 0 0
CUI: C0271932
Disease: Anemia of chronic renal failure
Anemia of chronic renal failure 		1 0 1 0.17 0 0
CUI: C0438921
Disease: Back Pain without Radiation
Back Pain without Radiation 		1 0 1 0.17 0 0
CUI: C0472713
Disease: Anemia of renal disease
Anemia of renal disease 		1 0 1 0.17 0 0
CUI: C0543645
Disease: Heterozygous hemoglobinopathy
Heterozygous hemoglobinopathy 		1 0 1 0.17 0 0
CUI: C0578736
Disease: Inguinal lymphadenopathy
Inguinal lymphadenopathy 		1 0 1 0.17 0 0
CUI: C0740363
Disease: Back Pain with Radiation
Back Pain with Radiation 		1 0 1 0.17 0 0
CUI: C0750949
Disease: Vertebrogenic Pain Syndrome
Vertebrogenic Pain Syndrome 		1 0 1 0.17 0 0
CUI: C0796159
Disease: Mental retardation Smith Fineman Myers type
Mental retardation Smith Fineman Myers type 		1 0 1 0.17 0 0
CUI: C0877172
Disease: Hematoma, Epidural, Spinal
Hematoma, Epidural, Spinal 		1 0 1 0.17 0 0
CUI: C0877243
Disease: Increased serum serotonin
Increased serum serotonin 		8 0 2 0.17 0 0
CUI: C0948437
Disease: Bone marrow dysplasia
Bone marrow dysplasia 		1 0 1 0.17 0 0
CUI: C1168215
Disease: Uremic anemia
Uremic anemia 		1 0 1 0.17 0 0
CUI: C1260334
Disease: Erythropoietin-resistant anemia
Erythropoietin-resistant anemia 		1 0 1 0.17 0 0