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: C0265490
Disease: Trisomy 22
Trisomy 22
5 0 2 0.22 0 0
CUI: C0178650
Disease: Gammopathy
Gammopathy
1 0 1 0.17 0 0
CUI: C0206672
Disease: Hidrocystoma
Hidrocystoma
1 0 1 0.17 0 0
Telangiectasia macularis eruptiva perstans
1 0 1 0.17 0 0
CUI: C0334432
Disease: Nonpigmented nevus
Nonpigmented nevus
1 0 1 0.17 0 0
CUI: C0341215
Disease: Gastroduodenal intussusception
Gastroduodenal intussusception
1 0 1 0.17 0 0
CUI: C0343115
Disease: Skin Mastocytoma
Skin Mastocytoma
1 0 1 0.17 0 0
CUI: C0413235
Disease: Idiopathic anaphylaxis
Idiopathic anaphylaxis
1 0 1 0.17 0 0
Acute promyelocytic leukemia, in remission
1 0 1 0.17 0 0
CUI: C1275345
Disease: Familial mastocytosis
Familial mastocytosis
1 0 1 0.17 0 0
CUI: C1333460
Disease: Esophageal Melanoma
Esophageal Melanoma
1 0 1 0.17 0 0
Gastrointestinal Stromal Tumor of the Gastrointestinal Tract
1 0 1 0.17 0 0
Intermediate Risk Gastrointestinal Stromal Tumor
1 0 1 0.17 0 0
Spindle Cell Type Gastrointestinal Stromal Tumor
1 0 1 0.17 0 0
Chronic myeloid leukemia in lymphoid blast crisis
1 0 1 0.17 0 0
adult acute myeloid leukemia with inv(16)(p13;q22)
1 0 1 0.17 0 0
GASTROINTESTINAL STROMAL TUMOR, FAMILIAL
1 0 1 0.17 0 0
B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged
1 0 1 0.17 0 0
CUI: C2931518
Disease: Plexosarcoma
Plexosarcoma
1 0 1 0.17 0 0
PIEBALDISM WITH SENSORINEURAL DEAFNESS
1 0 1 0.17 0 0
CUI: C4016297
Disease: PIEBALDISM, PROGRESSIVE
PIEBALDISM, PROGRESSIVE
1 0 1 0.17 0 0
CUI: C4038952
Disease: Metastatic thymic carcinoma
Metastatic thymic carcinoma
1 0 1 0.17 0 0
CUI: C4040134
Disease: Metastatic seminoma
Metastatic seminoma
1 0 1 0.17 0 0
Monoclonal mast cell activation syndrome
1 0 1 0.17 0 0
CUI: C4509020
Disease: Isolated bone marrow mastocytosis
Isolated bone marrow mastocytosis
1 0 1 0.17 0 0