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: C0917817
Disease: Neurofibromatosis 3
Neurofibromatosis 3 		5 0 4 0.21 0 0
CUI: C3273254
Disease: Arterionephrosclerosis
Arterionephrosclerosis 		11 0 5 0.21 0 0
CUI: C4048809
Disease: SCHWANNOMATOSIS 1
SCHWANNOMATOSIS 1 		3 0 3 0.17 0 0
CUI: C4024276
Disease: Peripheral Schwannoma
Peripheral Schwannoma 		4 0 3 0.16 0 0
CUI: C2931480
Disease: Neurofibromatosis, Type 3, mixed central and peripheral
Neurofibromatosis, Type 3, mixed central and peripheral 		15 0 4 0.14 0 0
CUI: C0347515
Disease: Spinal Meningioma
Spinal Meningioma 		19 0 4 0.12 0 0
CUI: C0265211
Disease: Marshall-Smith syndrome
Marshall-Smith syndrome 		2 0 2 0.11 0 0
CUI: C0280746
Disease: Sarcoma of ovary
Sarcoma of ovary 		3 0 2 0.11 0 0
CUI: C1334620
Disease: Malignant Smooth Muscle Neoplasm
Malignant Smooth Muscle Neoplasm 		3 0 2 0.11 0 0
CUI: C1968855
Disease: Paradoxical increased cortisol secretion on dexamethasone suppression test
Paradoxical increased cortisol secretion on dexamethasone suppression test 		3 0 2 0.11 0 0
CUI: C2985524
Disease: Rhabdoid tumor predisposition syndrome
Rhabdoid tumor predisposition syndrome 		3 0 2 0.11 0 0
CUI: C1136042
Disease: Neuroma, Acoustic, Bilateral
Neuroma, Acoustic, Bilateral 		4 0 2 1.0E-01 0 0
CUI: C1859436
Disease: Weak extraocular muscles
Weak extraocular muscles 		4 0 2 1.0E-01 0 0
CUI: C4022775
Disease: Focal T2 hypointense thalamic lesion
Focal T2 hypointense thalamic lesion 		4 0 2 1.0E-01 0 0
CUI: C4023215
Disease: Abnormality of central sensory function
Abnormality of central sensory function 		4 0 2 1.0E-01 0 0
CUI: C4054534
Disease: Meningioangiomatosis
Meningioangiomatosis 		4 0 2 1.0E-01 0 0
CUI: C4073063
Disease: Abnormal kinetic perimetry test
Abnormal kinetic perimetry test 		4 0 2 1.0E-01 0 0
CUI: C4552960
Disease: Ear Pain, CTCAE
Ear Pain, CTCAE 		4 0 2 1.0E-01 0 0
CUI: C0037930
Disease: Spinal Cord Neoplasms
Spinal Cord Neoplasms 		27 0 4 9.8E-02 0 0
CUI: C3280492
Disease: TUMOR PREDISPOSITION SYNDROME
TUMOR PREDISPOSITION SYNDROME 		16 0 3 9.7E-02 0 0
CUI: C0220998
Disease: Hypothalamic hypothyroidism
Hypothalamic hypothyroidism 		5 0 2 9.5E-02 0 0
CUI: C1334957
Disease: Neoplasm of the posterior pituitary
Neoplasm of the posterior pituitary 		5 0 2 9.5E-02 0 0
CUI: C3551915
Disease: MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO
MENINGIOMA, FAMILIAL, SUSCEPTIBILITY TO 		5 0 2 9.5E-02 0 0
CUI: C4072889
Disease: Decreased circulating follicle stimulating hormone level
Decreased circulating follicle stimulating hormone level 		5 0 2 9.5E-02 0 0
CUI: C4073006
Disease: Visual acuity test abnormality
Visual acuity test abnormality 		5 0 2 9.5E-02 0 0