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: C1851697
Disease: Pancreatic islet cell adenoma
Pancreatic islet cell adenoma 		1 0 1 4.0E-02 0 0
CUI: C1868000
Disease: Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal 		1 0 1 4.0E-02 0 0
CUI: C1868633
Disease: Paragangliomas with Sensorineural Hearing Loss
Paragangliomas with Sensorineural Hearing Loss 		1 0 1 4.0E-02 0 0
CUI: C1997262
Disease: Hypothyroidism in pregnancy
Hypothyroidism in pregnancy 		1 0 1 4.0E-02 0 0
CUI: C2362640
Disease: Neuronal choristoma
Neuronal choristoma 		1 0 1 4.0E-02 0 0
CUI: C2673187
Disease: Erythrocytosis, Familial, 4
Erythrocytosis, Familial, 4 		1 0 1 4.0E-02 0 0
CUI: C2674636
Disease: GASTROINTESTINAL STROMAL TUMOR, FAMILIAL
GASTROINTESTINAL STROMAL TUMOR, FAMILIAL 		1 0 1 4.0E-02 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 4.0E-02 0 0
CUI: C2931518
Disease: Plexosarcoma
Plexosarcoma 		1 0 1 4.0E-02 0 0
CUI: C3150898
Disease: CARDIOMYOPATHY, DILATED, 1GG
CARDIOMYOPATHY, DILATED, 1GG 		1 2 1 4.0E-02 1 0.14
CUI: C3276074
Disease: PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS
PARAGANGLIOMAS 1 WITH SENSORINEURAL HEARING LOSS 		1 0 1 4.0E-02 0 0
CUI: C3279992
Disease: PARAGANGLIOMAS 5
PARAGANGLIOMAS 5 		1 39 1 4.0E-02 1 2.3E-02
CUI: C3280094
Disease: PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3
PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 3 		1 0 1 4.0E-02 0 0
CUI: C3532243
Disease: Fatal infantile mitochondrial cardiomyopathy
Fatal infantile mitochondrial cardiomyopathy 		1 0 1 4.0E-02 0 0
CUI: C4016294
Disease: PIEBALDISM WITH SENSORINEURAL DEAFNESS
PIEBALDISM WITH SENSORINEURAL DEAFNESS 		1 0 1 4.0E-02 0 0
CUI: C4016297
Disease: PIEBALDISM, PROGRESSIVE
PIEBALDISM, PROGRESSIVE 		1 0 1 4.0E-02 0 0
CUI: C4016331
Disease: HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC, RESISTANT TO IMATINIB
HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC, RESISTANT TO IMATINIB 		1 0 1 4.0E-02 0 0
CUI: C4017330
Disease: LIPOMA, SOMATIC
LIPOMA, SOMATIC 		1 0 1 4.0E-02 0 0
CUI: C4017331
Disease: ANGIOFIBROMA, SOMATIC
ANGIOFIBROMA, SOMATIC 		1 0 1 4.0E-02 0 0
CUI: C4017332
Disease: ADRENAL ADENOMA, SOMATIC
ADRENAL ADENOMA, SOMATIC 		1 0 1 4.0E-02 0 0
CUI: C4022005
Disease: Carotid paraganglioma
Carotid paraganglioma 		1 0 1 4.0E-02 0 0
CUI: C4023669
Disease: Hypersarcosinuria
Hypersarcosinuria 		1 0 1 4.0E-02 0 0
CUI: C4024947
Disease: Symmetric lesions of the basal ganglia
Symmetric lesions of the basal ganglia 		1 0 1 4.0E-02 0 0
CUI: C4038952
Disease: Metastatic thymic carcinoma
Metastatic thymic carcinoma 		1 0 1 4.0E-02 0 0
CUI: C4040134
Disease: Metastatic seminoma
Metastatic seminoma 		1 0 1 4.0E-02 0 0