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: C1859436
Disease: Weak extraocular muscles
Weak extraocular muscles 		4 0 4 0.67 0 0
CUI: C4022775
Disease: Focal T2 hypointense thalamic lesion
Focal T2 hypointense thalamic lesion 		4 0 4 0.67 0 0
CUI: C4023215
Disease: Abnormality of central sensory function
Abnormality of central sensory function 		4 0 4 0.67 0 0
CUI: C4073063
Disease: Abnormal kinetic perimetry test
Abnormal kinetic perimetry test 		4 0 4 0.67 0 0
CUI: C4552960
Disease: Ear Pain, CTCAE
Ear Pain, CTCAE 		4 0 4 0.67 0 0
CUI: C0220998
Disease: Hypothalamic hypothyroidism
Hypothalamic hypothyroidism 		5 0 4 0.57 0 0
CUI: C1334957
Disease: Neoplasm of the posterior pituitary
Neoplasm of the posterior pituitary 		5 0 4 0.57 0 0
CUI: C4072889
Disease: Decreased circulating follicle stimulating hormone level
Decreased circulating follicle stimulating hormone level 		5 0 4 0.57 0 0
CUI: C4073006
Disease: Visual acuity test abnormality
Visual acuity test abnormality 		5 0 4 0.57 0 0
CUI: C0013456
Disease: Earache
Earache 		6 0 4 0.50 0 0
CUI: C0476405
Disease: Lung function testing abnormal
Lung function testing abnormal 		6 0 4 0.50 0 0
CUI: C4021206
Disease: Chromosomal breakage induced by ionizing radiation
Chromosomal breakage induced by ionizing radiation 		6 0 4 0.50 0 0
CUI: C4023205
Disease: Neoplasm of the anterior pituitary
Neoplasm of the anterior pituitary 		6 0 4 0.50 0 0
CUI: C4072890
Disease: Decreased circulating luteinizing hormone level
Decreased circulating luteinizing hormone level 		6 0 4 0.50 0 0
CUI: C0270680
Disease: Posterior fossa compression syndrome
Posterior fossa compression syndrome 		7 0 4 0.44 0 0
CUI: C4021850
Disease: Increased sensitivity to ionizing radiation
Increased sensitivity to ionizing radiation 		7 0 4 0.44 0 0
CUI: C0278152
Disease: Hemifacial Spasm
Hemifacial Spasm 		8 0 4 0.40 0 0
CUI: C0342422
Disease: Pituitary gland enlarged
Pituitary gland enlarged 		8 0 4 0.40 0 0
CUI: C3551915
Disease: MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO
MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO 		5 0 3 0.38 0 0
CUI: C0221184
Disease: Bitemporal Hemianopia
Bitemporal Hemianopia 		9 0 4 0.36 0 0
CUI: C1333989
Disease: Familial meningioma
Familial meningioma 		6 0 3 0.33 0 0
CUI: C4024716
Disease: Secondary growth hormone deficiency
Secondary growth hormone deficiency 		11 0 4 0.31 0 0
CUI: C4022395
Disease: Abnormality of the mediastinum
Abnormality of the mediastinum 		12 0 4 0.29 0 0
CUI: C4048809
Disease: SCHWANNOMATOSIS 1
SCHWANNOMATOSIS 1 		3 0 2 0.29 0 0
CUI: C4021655
Disease: Abnormality of the sense of smell
Abnormality of the sense of smell 		14 0 4 0.25 0 0