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: C0236960
Disease: Dementia due to Parkinson's disease
Dementia due to Parkinson's disease 		1 0 1 0.33 0 0
CUI: C0334113
Disease: Eosinophilic granulomatous polyp
Eosinophilic granulomatous polyp 		1 0 1 0.33 0 0
CUI: C0948384
Disease: Cerebral hygroma
Cerebral hygroma 		1 0 1 0.33 0 0
CUI: C1843164
Disease: Charcot-Marie-Tooth disease, demyelinating, Type 1F
Charcot-Marie-Tooth disease, demyelinating, Type 1F 		1 0 1 0.33 0 0
CUI: C1843169
Disease: Clusters of axonal regeneration
Clusters of axonal regeneration 		1 0 1 0.33 0 0
CUI: C1843225
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2E (disorder) 		1 0 1 0.33 0 0
CUI: C1868000
Disease: Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal 		1 0 1 0.33 0 0
CUI: C1970250
Disease: Prostate Cancer, Hereditary, 9
Prostate Cancer, Hereditary, 9 		1 0 1 0.33 0 0
CUI: C4016331
Disease: HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC, RESISTANT TO IMATINIB
HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC, RESISTANT TO IMATINIB 		1 0 1 0.33 0 0
CUI: C4545381
Disease: Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement
Myeloid and/or lymphoid neoplasm associated with platelet derived growth factor receptor alpha rearrangement 		1 0 1 0.33 0 0
CUI: C4693509
Disease: CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G
CHARCOT-MARIE-TOOTH DISEASE, DOMINANT INTERMEDIATE G 		1 0 1 0.33 0 0
CUI: C4749824
Disease: Charcot-Marie-Tooth disease type 2B5
Charcot-Marie-Tooth disease type 2B5 		1 0 1 0.33 0 0
CUI: C0205769
Disease: Myxopapillary ependymoma
Myxopapillary ependymoma 		12 0 3 0.25 0 0
CUI: C0206143
Disease: Loeffler's Endocarditis
Loeffler's Endocarditis 		2 0 1 0.25 0 0
CUI: C0281328
Disease: Adult Subependymoma
Adult Subependymoma 		7 0 2 0.25 0 0
CUI: C0544799
Disease: Histiocytosis, generalized eruptive
Histiocytosis, generalized eruptive 		2 0 1 0.25 0 0
CUI: C1290854
Disease: Disorder of skull
Disorder of skull 		2 0 1 0.25 0 0
CUI: C1302645
Disease: Polyp of small intestine
Polyp of small intestine 		2 0 1 0.25 0 0
CUI: C1334378
Disease: Laryngeal Small Cell Carcinoma
Laryngeal Small Cell Carcinoma 		2 0 1 0.25 0 0
CUI: C1516858
Disease: Endometrial Small Cell Carcinoma
Endometrial Small Cell Carcinoma 		2 0 1 0.25 0 0
CUI: C1843228
Disease: Hypotrophy of the small hand muscles
Hypotrophy of the small hand muscles 		2 0 1 0.25 0 0
CUI: C2930862
Disease: Primary angiitis of the central nervous system
Primary angiitis of the central nervous system 		2 0 1 0.25 0 0
CUI: C4733337
Disease: hereditary gastrointestinal stromal tumor
hereditary gastrointestinal stromal tumor 		2 0 1 0.25 0 0
CUI: C4723619
Disease: Brain Ependymoma
Brain Ependymoma 		8 0 2 0.22 0 0
CUI: C0035238
Disease: Congenital abnormality of respiratory system
Congenital abnormality of respiratory system 		3 0 1 0.20 0 0