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: C0039234
Disease: Tachycardia, Ectopic Atrial
Tachycardia, Ectopic Atrial 		3 0 2 0.40 0 0
CUI: C2609093
Disease: Pancreatic neuroendocrine tumour metastatic
Pancreatic neuroendocrine tumour metastatic 		5 0 2 0.29 0 0
CUI: C0010334
Disease: Crisscross Heart
Crisscross Heart 		1 0 1 0.25 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 0.25 0 0
CUI: C0178650
Disease: Gammopathy
Gammopathy 		1 0 1 0.25 0 0
CUI: C0206672
Disease: Hidrocystoma
Hidrocystoma 		1 0 1 0.25 0 0
CUI: C0232259
Disease: Mid-systolic murmur
Mid-systolic murmur 		1 0 1 0.25 0 0
CUI: C0263402
Disease: Telangiectasia macularis eruptiva perstans
Telangiectasia macularis eruptiva perstans 		1 0 1 0.25 0 0
CUI: C0334432
Disease: Nonpigmented nevus
Nonpigmented nevus 		1 0 1 0.25 0 0
CUI: C0341215
Disease: Gastroduodenal intussusception
Gastroduodenal intussusception 		1 0 1 0.25 0 0
CUI: C0343115
Disease: Skin Mastocytoma
Skin Mastocytoma 		1 0 1 0.25 0 0
CUI: C0349477
Disease: Transient neonatal hypothyroidism
Transient neonatal hypothyroidism 		1 0 1 0.25 0 0
CUI: C0409939
Disease: Osteoarthritis of glenohumeral joint
Osteoarthritis of glenohumeral joint 		1 0 1 0.25 0 0
CUI: C0413235
Disease: Idiopathic anaphylaxis
Idiopathic anaphylaxis 		1 0 1 0.25 0 0
CUI: C0553668
Disease: Labored breathing
Labored breathing 		1 0 1 0.25 0 0
CUI: C1275345
Disease: Familial mastocytosis
Familial mastocytosis 		1 0 1 0.25 0 0
CUI: C1333460
Disease: Esophageal Melanoma
Esophageal Melanoma 		1 0 1 0.25 0 0
CUI: C1333802
Disease: Gastrointestinal Stromal Tumor of the Gastrointestinal Tract
Gastrointestinal Stromal Tumor of the Gastrointestinal Tract 		1 0 1 0.25 0 0
CUI: C1334222
Disease: Intermediate Risk Gastrointestinal Stromal Tumor
Intermediate Risk Gastrointestinal Stromal Tumor 		1 0 1 0.25 0 0
CUI: C1336056
Disease: Spindle Cell Type Gastrointestinal Stromal Tumor
Spindle Cell Type Gastrointestinal Stromal Tumor 		1 0 1 0.25 0 0
CUI: C1541333
Disease: adult acute myeloid leukemia with inv(16)(p13;q22)
adult acute myeloid leukemia with inv(16)(p13;q22) 		1 0 1 0.25 0 0
CUI: C1834056
Disease: Thin anteverted nares
Thin anteverted nares 		1 0 1 0.25 0 0
CUI: C1834057
Disease: Vertebral hyperostosis
Vertebral hyperostosis 		1 0 1 0.25 0 0
CUI: C1857508
Disease: Patchy sclerosis of finger phalanx
Patchy sclerosis of finger phalanx 		1 0 1 0.25 0 0
CUI: C1861366
Disease: SYNDACTYLY, TYPE III
SYNDACTYLY, TYPE III 		1 0 1 0.25 0 0