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: C4318479
Disease: Growth Hormone Insensitivity Syndrome
Growth Hormone Insensitivity Syndrome 		4 0 4 0.20 0 0
CUI: C1845118
Disease: SHORT STATURE, IDIOPATHIC, X-LINKED
SHORT STATURE, IDIOPATHIC, X-LINKED 		18 0 6 0.19 0 0
CUI: C0271568
Disease: Laron Syndrome
Laron Syndrome 		20 0 6 0.18 0 0
CUI: C3897045
Disease: Short Stature Homeobox Deficiency
Short Stature Homeobox Deficiency 		8 0 4 0.17 0 0
CUI: C0858734
Disease: Insulin hypoglycemia
Insulin hypoglycemia 		5 0 3 0.14 0 0
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder) 		16 42 4 0.12 1 2.4E-02
CUI: C0026707
Disease: Mucopolysaccharidosis IV
Mucopolysaccharidosis IV 		28 0 5 0.12 0 0
CUI: C1837475
Disease: Insulin-Like Growth Factor I Deficiency
Insulin-Like Growth Factor I Deficiency 		28 0 5 0.12 0 0
CUI: C0349208
Disease: Manic episode
Manic episode 		9 0 3 0.12 0 0
CUI: C1855538
Disease: Small face
Small face 		10 0 3 0.11 0 0
CUI: C0342543
Disease: Central Precocious Puberty
Central Precocious Puberty 		32 0 5 0.11 0 0
CUI: C0878787
Disease: Growth failure
Growth failure 		84 0 10 0.11 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 21 6 1.0E-01 1 4.8E-02
CUI: C0271547
Disease: Overproduction of growth hormone
Overproduction of growth hormone 		2 0 2 1.0E-01 0 0
CUI: C0281913
Disease: Swelling of skeletal muscle
Swelling of skeletal muscle 		2 0 2 1.0E-01 0 0
CUI: C1867487
Disease: Childhood onset short-limb short stature
Childhood onset short-limb short stature 		2 0 2 1.0E-01 0 0
CUI: C1835473
Disease: Diaphyseal thickening
Diaphyseal thickening 		14 0 3 9.7E-02 0 0
CUI: C0795855
Disease: Ring chromosome 15 syndrome
Ring chromosome 15 syndrome 		3 0 2 9.5E-02 0 0
CUI: C1261982
Disease: Chondrosis
Chondrosis 		3 0 2 9.5E-02 0 0
CUI: C1866239
Disease: Mesomelic/rhizomelic limb shortening
Mesomelic/rhizomelic limb shortening 		3 0 2 9.5E-02 0 0
CUI: C2748571
Disease: Isolated Growth Hormone Deficiency, Type IB
Isolated Growth Hormone Deficiency, Type IB 		3 0 2 9.5E-02 0 0
CUI: C4722273
Disease: ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV
ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV 		3 0 2 9.5E-02 0 0
CUI: C0549306
Disease: Mesomelia
Mesomelia 		27 0 4 9.3E-02 0 0
CUI: C0014008
Disease: Empty Sella Syndrome
Empty Sella Syndrome 		4 0 2 9.1E-02 0 0
CUI: C0271695
Disease: Rabson-Mendenhall Syndrome
Rabson-Mendenhall Syndrome 		4 0 2 9.1E-02 0 0