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: C0271547
Disease: Overproduction of growth hormone
Overproduction of growth hormone 		2 0 2 0.29 0 0
CUI: C0281913
Disease: Swelling of skeletal muscle
Swelling of skeletal muscle 		2 0 2 0.29 0 0
CUI: C0014008
Disease: Empty Sella Syndrome
Empty Sella Syndrome 		4 0 2 0.22 0 0
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
Rabson-Mendenhall Syndrome 		4 0 2 0.22 0 0
CUI: C4318479
Disease: Growth Hormone Insensitivity Syndrome
Growth Hormone Insensitivity Syndrome 		4 0 2 0.22 0 0
CUI: C4543877
Disease: Osteopenia due to disuse
Osteopenia due to disuse 		4 0 2 0.22 0 0
CUI: C0405578
Disease: Gigantism and acromegaly
Gigantism and acromegaly 		5 0 2 0.20 0 0
CUI: C0858734
Disease: Insulin hypoglycemia
Insulin hypoglycemia 		5 0 2 0.20 0 0
CUI: C1455734
Disease: Congenital hypoparathyroidism
Congenital hypoparathyroidism 		5 0 2 0.20 0 0
CUI: C1849524
Disease: Pygmy (disorder)
Pygmy (disorder) 		5 0 2 0.20 0 0
CUI: C0740749
Disease: Chronic metabolic acidosis
Chronic metabolic acidosis 		6 0 2 0.18 0 0
CUI: C1720505
Disease: Adult growth hormone deficiency
Adult growth hormone deficiency 		6 0 2 0.18 0 0
CUI: C1971021
Disease: Potassium depletion
Potassium depletion 		6 0 2 0.18 0 0
CUI: C0264009
Disease: Osteodystrophy
Osteodystrophy 		7 0 2 0.17 0 0
CUI: C3891556
Disease: CHROMOSOME Xq26.3 DUPLICATION SYNDROME
CHROMOSOME Xq26.3 DUPLICATION SYNDROME 		8 0 2 0.15 0 0
CUI: C3897045
Disease: Short Stature Homeobox Deficiency
Short Stature Homeobox Deficiency 		8 0 2 0.15 0 0
CUI: C0018121
Disease: Gradenigo Syndrome
Gradenigo Syndrome 		1 0 1 0.14 0 0
CUI: C0026686
Disease: Mucocele of salivary gland
Mucocele of salivary gland 		1 0 1 0.14 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 0.14 0 0
CUI: C0155804
Disease: Acute maxillary sinusitis
Acute maxillary sinusitis 		1 0 1 0.14 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 0.14 0 0
CUI: C0242012
Disease: NEPHROTIC SYNDROME, CHRONIC
NEPHROTIC SYNDROME, CHRONIC 		1 0 1 0.14 0 0
CUI: C0264622
Disease: Psychogenic voice disorder
Psychogenic voice disorder 		1 0 1 0.14 0 0
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		1 0 1 0.14 0 0
CUI: C0271848
Disease: Hyperparathyroidism due to vitamin D deficiency
Hyperparathyroidism due to vitamin D deficiency 		1 0 1 0.14 0 0