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: C0346328
Disease: Meningioma of optic nerve sheath
Meningioma of optic nerve sheath 		1 0 1 0.20 0 0
CUI: C0349529
Disease: Gastric Carcinoid Tumor
Gastric Carcinoid Tumor 		1 0 1 0.20 0 0
CUI: C0678053
Disease: Stage IV Adrenal Cortex Carcinoma AJCC v7
Stage IV Adrenal Cortex Carcinoma AJCC v7 		1 0 1 0.20 0 0
CUI: C0851362
Disease: General disorders and administration site conditions
General disorders and administration site conditions 		1 0 1 0.20 0 0
CUI: C0940958
Disease: angioectasia
angioectasia 		1 0 1 0.20 0 0
CUI: C1835666
Disease: Hyperkeratosis, diffuse palmoplantar (tylosis)
Hyperkeratosis, diffuse palmoplantar (tylosis) 		1 0 1 0.20 0 0
CUI: C2609042
Disease: Post embolisation syndrome
Post embolisation syndrome 		1 0 1 0.20 0 0
CUI: C3280501
Disease: INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1
INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 1 		1 0 1 0.20 0 0
CUI: C4518348
Disease: Ectopic pituitary adenoma
Ectopic pituitary adenoma 		1 0 1 0.20 0 0
CUI: C4724971
Disease: Refractory Sarcoma
Refractory Sarcoma 		1 0 1 0.20 0 0
CUI: C4725028
Disease: Unresectable Intrahepatic Cholangiocarcinoma
Unresectable Intrahepatic Cholangiocarcinoma 		1 0 1 0.20 0 0
CUI: C1833030
Disease: PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC
PALMOPLANTAR KERATODERMA, NONEPIDERMOLYTIC 		8 0 2 0.18 0 0
CUI: C0007093
Disease: Carcinoid Heart Disease
Carcinoid Heart Disease 		2 0 1 0.17 0 0
CUI: C0013288
Disease: Dumping Syndrome
Dumping Syndrome 		2 0 1 0.17 0 0
CUI: C0221243
Disease: Necrolytic Migratory Erythema
Necrolytic Migratory Erythema 		2 0 1 0.17 0 0
CUI: C0342569
Disease: Carcinoid crisis
Carcinoid crisis 		2 0 1 0.17 0 0
CUI: C0496901
Disease: Benign neoplasm of pituitary gland
Benign neoplasm of pituitary gland 		2 0 1 0.17 0 0
CUI: C0948141
Disease: Hepatic cyst infection
Hepatic cyst infection 		2 0 1 0.17 0 0
CUI: C1335096
Disease: Occult Lung Adenocarcinoma
Occult Lung Adenocarcinoma 		2 0 1 0.17 0 0
CUI: C1845117
Disease: Immunodeficiency without anhidrotic ectodermal dysplasia
Immunodeficiency without anhidrotic ectodermal dysplasia 		2 0 1 0.17 0 0
CUI: C1970879
Disease: ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 1 (disorder)
ATYPICAL MYCOBACTERIOSIS, FAMILIAL, X-LINKED 1 (disorder) 		2 0 1 0.17 0 0
CUI: C3489771
Disease: Keratosis Palmaris et Plantaris Familiaris
Keratosis Palmaris et Plantaris Familiaris 		2 0 1 0.17 0 0
CUI: C3827733
Disease: Umbilical cord occlusion
Umbilical cord occlusion 		2 0 1 0.17 0 0
CUI: C4021575
Disease: Diffuse palmoplantar hyperkeratosis
Diffuse palmoplantar hyperkeratosis 		2 0 1 0.17 0 0
CUI: C4025715
Disease: Abnormal large intestine morphology
Abnormal large intestine morphology 		2 0 1 0.17 0 0