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: C0178650
Disease: Gammopathy
Gammopathy 		1 0 1 0.12 0 0
CUI: C0206672
Disease: Hidrocystoma
Hidrocystoma 		1 0 1 0.12 0 0
CUI: C0263402
Disease: Telangiectasia macularis eruptiva perstans
Telangiectasia macularis eruptiva perstans 		1 0 1 0.12 0 0
CUI: C0334432
Disease: Nonpigmented nevus
Nonpigmented nevus 		1 0 1 0.12 0 0
CUI: C0341215
Disease: Gastroduodenal intussusception
Gastroduodenal intussusception 		1 0 1 0.12 0 0
CUI: C0343115
Disease: Skin Mastocytoma
Skin Mastocytoma 		1 0 1 0.12 0 0
CUI: C0375536
Disease: Congenital osteodystrophy
Congenital osteodystrophy 		1 0 1 0.12 0 0
CUI: C0413235
Disease: Idiopathic anaphylaxis
Idiopathic anaphylaxis 		1 0 1 0.12 0 0
CUI: C1275345
Disease: Familial mastocytosis
Familial mastocytosis 		1 0 1 0.12 0 0
CUI: C1333460
Disease: Esophageal Melanoma
Esophageal Melanoma 		1 0 1 0.12 0 0
CUI: C1333802
Disease: Gastrointestinal Stromal Tumor of the Gastrointestinal Tract
Gastrointestinal Stromal Tumor of the Gastrointestinal Tract 		1 0 1 0.12 0 0
CUI: C1334222
Disease: Intermediate Risk Gastrointestinal Stromal Tumor
Intermediate Risk Gastrointestinal Stromal Tumor 		1 0 1 0.12 0 0
CUI: C1336056
Disease: Spindle Cell Type Gastrointestinal Stromal Tumor
Spindle Cell Type Gastrointestinal Stromal Tumor 		1 0 1 0.12 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 0.12 0 0
CUI: C1837203
Disease: WAARDENBURG SYNDROME, TYPE IID
WAARDENBURG SYNDROME, TYPE IID 		1 0 1 0.12 0 0
CUI: C1851988
Disease: Dorsal subluxation of ulna
Dorsal subluxation of ulna 		1 0 1 0.12 0 0
CUI: C1855276
Disease: Dorsolateral bowed, short radii
Dorsolateral bowed, short radii 		1 0 1 0.12 0 0
CUI: C1857652
Disease: Thymic hormone decreased
Thymic hormone decreased 		1 0 1 0.12 0 0
CUI: C2674636
Disease: GASTROINTESTINAL STROMAL TUMOR, FAMILIAL
GASTROINTESTINAL STROMAL TUMOR, FAMILIAL 		1 0 1 0.12 0 0
CUI: C2698309
Disease: B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged
B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged 		1 0 1 0.12 0 0
CUI: C2931518
Disease: Plexosarcoma
Plexosarcoma 		1 0 1 0.12 0 0
CUI: C3151403
Disease: AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 		1 0 1 0.12 0 0
CUI: C3152097
Disease: AMYOTROPHIC LATERAL SCLEROSIS 14 WITHOUT FRONTOTEMPORAL DEMENTIA
AMYOTROPHIC LATERAL SCLEROSIS 14 WITHOUT FRONTOTEMPORAL DEMENTIA 		1 0 1 0.12 0 0
CUI: C3553298
Disease: UV-SENSITIVE SYNDROME 2
UV-SENSITIVE SYNDROME 2 		1 0 1 0.12 0 0
CUI: C3809469
Disease: INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA 3 		1 0 1 0.12 0 0