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: C4022676
Disease: Decreased female libido
Decreased female libido 		4 0 3 0.43 0 0
CUI: C4023401
Disease: Abnormality of hair density
Abnormality of hair density 		4 0 3 0.43 0 0
CUI: C0339693
Disease: Internal Ophthalmoplegia
Internal Ophthalmoplegia 		5 0 3 0.38 0 0
CUI: C4072828
Disease: Sudden loss of visual acuity
Sudden loss of visual acuity 		5 0 3 0.38 0 0
CUI: C1863340
Disease: PITUITARY ADENOMA PREDISPOSITION (disorder)
PITUITARY ADENOMA PREDISPOSITION (disorder) 		2 0 2 0.33 0 0
CUI: C3665358
Disease: Galactorrhea
Galactorrhea 		6 0 3 0.33 0 0
CUI: C4552171
Disease: Familial acromegaly
Familial acromegaly 		3 0 2 0.29 0 0
CUI: C4551519
Disease: Abducens Nerve Palsy
Abducens Nerve Palsy 		8 0 3 0.27 0 0
CUI: C0221184
Disease: Bitemporal Hemianopia
Bitemporal Hemianopia 		9 0 3 0.25 0 0
CUI: C4024716
Disease: Secondary growth hormone deficiency
Secondary growth hormone deficiency 		11 0 3 0.21 0 0
CUI: C0342388
Disease: Adrenocorticotropic hormone (ACTH) deficiency (disorder)
Adrenocorticotropic hormone (ACTH) deficiency (disorder) 		24 0 5 0.20 0 0
CUI: C4025669
Disease: Decreased circulating ACTH level
Decreased circulating ACTH level 		18 0 4 0.20 0 0
CUI: C0271375
Disease: Fourth cranial nerve paresis
Fourth cranial nerve paresis 		13 0 3 0.19 0 0
CUI: C0276429
Disease: Enteroviral encephalomyelitis
Enteroviral encephalomyelitis 		1 0 1 0.17 0 0
CUI: C0338401
Disease: Enteroviral encephalitis
Enteroviral encephalitis 		1 0 1 0.17 0 0
CUI: C1400201
Disease: Pituitary anomalies
Pituitary anomalies 		1 0 1 0.17 0 0
CUI: C1851697
Disease: Pancreatic islet cell adenoma
Pancreatic islet cell adenoma 		1 0 1 0.17 0 0
CUI: C2362640
Disease: Neuronal choristoma
Neuronal choristoma 		1 0 1 0.17 0 0
CUI: C3152102
Disease: USH1D/F, CDH23/PCDH15, DIGENIC
USH1D/F, CDH23/PCDH15, DIGENIC 		1 0 1 0.17 0 0
CUI: C3275872
Disease: USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC
USHER SYNDROME, TYPE ID/F, CDH23/PCDH15, DIGENIC 		1 0 1 0.17 0 0
CUI: C4017330
Disease: LIPOMA, SOMATIC
LIPOMA, SOMATIC 		1 0 1 0.17 0 0
CUI: C4017331
Disease: ANGIOFIBROMA, SOMATIC
ANGIOFIBROMA, SOMATIC 		1 0 1 0.17 0 0
CUI: C4017332
Disease: ADRENAL ADENOMA, SOMATIC
ADRENAL ADENOMA, SOMATIC 		1 0 1 0.17 0 0
CUI: C4018860
Disease: Pituitary growth hormone cell adenoma
Pituitary growth hormone cell adenoma 		8 0 2 0.17 0 0
CUI: C4021549
Disease: Euthyroid hyperthyroxinemia
Euthyroid hyperthyroxinemia 		1 0 1 0.17 0 0