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: C1846550
Disease: Decreased T cell activation
Decreased T cell activation 		6 0 2 0.17 0 0
CUI: C0220989
Disease: Acquired partial lipodystrophy
Acquired partial lipodystrophy 		7 0 2 0.15 0 0
CUI: C1449647
Disease: Secondary Peritonitis
Secondary Peritonitis 		8 0 2 0.14 0 0
CUI: C1504375
Disease: Diabetic macroangiopathy
Diabetic macroangiopathy 		9 0 2 0.13 0 0
CUI: C1720863
Disease: Congenital Generalized Lipodystrophy Type 2
Congenital Generalized Lipodystrophy Type 2 		9 0 2 0.13 0 0
CUI: C3554225
Disease: LEPTIN RECEPTOR DEFICIENCY
LEPTIN RECEPTOR DEFICIENCY 		9 0 2 0.13 0 0
CUI: C4505163
Disease: Food Addiction
Food Addiction 		9 0 2 0.13 0 0
CUI: C0005911
Disease: Body Weight Changes
Body Weight Changes 		1 0 1 0.12 0 0
CUI: C0028949
Disease: Oligomenorrhea
Oligomenorrhea 		37 0 5 0.12 0 0
CUI: C0037188
Disease: Sinoatrial Block
Sinoatrial Block 		1 0 1 0.12 0 0
CUI: C0238110
Disease: Chronic epididymitis
Chronic epididymitis 		1 0 1 0.12 0 0
CUI: C0267896
Disease: Mucocele of gallbladder
Mucocele of gallbladder 		1 0 1 0.12 0 0
CUI: C0751437
Disease: Adenohypophyseal Diseases
Adenohypophyseal Diseases 		1 0 1 0.12 0 0
CUI: C0751438
Disease: Posterior pituitary disease
Posterior pituitary disease 		1 0 1 0.12 0 0
CUI: C0796031
Disease: Malouf syndrome
Malouf syndrome 		1 0 1 0.12 0 0
CUI: C0796083
Disease: Najjar syndrome
Najjar syndrome 		1 0 1 0.12 0 0
CUI: C0948393
Disease: Oedematous pancreatitis
Oedematous pancreatitis 		1 0 1 0.12 0 0
CUI: C1835380
Disease: Labial pseudohypertrophy
Labial pseudohypertrophy 		1 0 1 0.12 0 0
CUI: C1835389
Disease: Increased intramuscular fat
Increased intramuscular fat 		1 0 1 0.12 0 0
CUI: C1857829
Disease: Heart-hand syndrome, Slovenian type
Heart-hand syndrome, Slovenian type 		1 0 1 0.12 0 0
CUI: C2675074
Disease: Enlarged peripheral nerve
Enlarged peripheral nerve 		1 0 1 0.12 0 0
CUI: C2750035
Disease: Emery-Dreifuss Muscular Dystrophy 3
Emery-Dreifuss Muscular Dystrophy 3 		1 0 1 0.12 0 0
CUI: C2750285
Disease: Progeria Syndrome, Childhood-Onset
Progeria Syndrome, Childhood-Onset 		1 0 1 0.12 0 0
CUI: C2750785
Disease: MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder)
MUSCULAR DYSTROPHY, CONGENITAL, LMNA-RELATED (disorder) 		1 0 1 0.12 0 0
CUI: C3249879
Disease: Combat Fatigue
Combat Fatigue 		1 0 1 0.12 0 0