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: C3891556
Disease: CHROMOSOME Xq26.3 DUPLICATION SYNDROME
CHROMOSOME Xq26.3 DUPLICATION SYNDROME 		8 0 4 0.44 0 0
CUI: C0271547
Disease: Overproduction of growth hormone
Overproduction of growth hormone 		2 0 2 0.40 0 0
CUI: C0281913
Disease: Swelling of skeletal muscle
Swelling of skeletal muscle 		2 0 2 0.40 0 0
CUI: C4025548
Disease: Cortical diaphyseal thickening of the upper limbs
Cortical diaphyseal thickening of the upper limbs 		2 0 2 0.40 0 0
CUI: C4022551
Disease: Wide penis
Wide penis 		3 0 2 0.33 0 0
CUI: C0014008
Disease: Empty Sella Syndrome
Empty Sella Syndrome 		4 0 2 0.29 0 0
CUI: C0020494
Disease: Hyperostosis Frontalis Interna
Hyperostosis Frontalis Interna 		4 0 2 0.29 0 0
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
Rabson-Mendenhall Syndrome 		4 0 2 0.29 0 0
CUI: C4318479
Disease: Growth Hormone Insensitivity Syndrome
Growth Hormone Insensitivity Syndrome 		4 0 2 0.29 0 0
CUI: C0858734
Disease: Insulin hypoglycemia
Insulin hypoglycemia 		5 0 2 0.25 0 0
CUI: C1849524
Disease: Pygmy (disorder)
Pygmy (disorder) 		5 0 2 0.25 0 0
CUI: C0017547
Disease: Gigantism
Gigantism 		16 0 4 0.24 0 0
CUI: C0740749
Disease: Chronic metabolic acidosis
Chronic metabolic acidosis 		6 0 2 0.22 0 0
CUI: C1720505
Disease: Adult growth hormone deficiency
Adult growth hormone deficiency 		6 0 2 0.22 0 0
CUI: C1971021
Disease: Potassium depletion
Potassium depletion 		6 0 2 0.22 0 0
CUI: C3281059
Disease: Broad jaw
Broad jaw 		6 0 2 0.22 0 0
CUI: C3665358
Disease: Galactorrhea
Galactorrhea 		6 0 2 0.22 0 0
CUI: C0269011
Disease: Increased size of penis
Increased size of penis 		12 0 3 0.21 0 0
CUI: C3489630
Disease: Somatotrophinoma, Familial
Somatotrophinoma, Familial 		18 0 4 0.21 0 0
CUI: C0016064
Disease: Fibrous Dysplasia, Monostotic
Fibrous Dysplasia, Monostotic 		1 0 1 0.20 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 0.20 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 0.20 0 0
CUI: C0206642
Disease: Parosteal Osteosarcoma
Parosteal Osteosarcoma 		7 0 2 0.20 0 0
CUI: C0238402
Disease: Pycnodysostosis
Pycnodysostosis 		7 0 2 0.20 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 0.20 0 0