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: C0342841
Disease: Hunter's syndrome, severe form
Hunter's syndrome, severe form 		1 0 1 1.00 0 0
CUI: C0342842
Disease: Hunter's syndrome, mild form
Hunter's syndrome, mild form 		1 0 1 1.00 0 0
CUI: C4552512
Disease: Neurocognitive deficit
Neurocognitive deficit 		1 0 1 1.00 0 0
CUI: C0679047
Disease: perseverative thinking
perseverative thinking 		2 0 1 0.50 0 0
CUI: C1096378
Disease: Near sudden infant death syndrome
Near sudden infant death syndrome 		2 0 1 0.50 0 0
CUI: C4025598
Disease: Urinary glycosaminoglycan excretion
Urinary glycosaminoglycan excretion 		2 0 1 0.50 0 0
CUI: C1854774
Disease: Dermatan sulfate excretion in urine
Dermatan sulfate excretion in urine 		3 0 1 0.33 0 0
CUI: C0852866
Disease: Cervical cord compression
Cervical cord compression 		4 0 1 0.25 0 0
CUI: C0340231
Disease: Tracheobronchomalacia
Tracheobronchomalacia 		6 0 1 0.17 0 0
CUI: C1313952
Disease: Respiration intermittent
Respiration intermittent 		6 0 1 0.17 0 0
CUI: C0342791
Disease: Carnitine-Acylcarnitine Translocase Deficiency
Carnitine-Acylcarnitine Translocase Deficiency 		7 0 1 0.14 0 0
CUI: C1854827
Disease: Heparan sulfate excretion in urine
Heparan sulfate excretion in urine 		7 0 1 0.14 0 0
CUI: C0026709
Disease: Mucopolysaccharidosis VI
Mucopolysaccharidosis VI 		11 0 1 9.1E-02 0 0
CUI: C1536075
Disease: Sudden unexplained death in epilepsy
Sudden unexplained death in epilepsy 		12 0 1 8.3E-02 0 0
CUI: C1833661
Disease: PAROXYSMAL EXTREME PAIN DISORDER
PAROXYSMAL EXTREME PAIN DISORDER 		13 0 1 7.7E-02 0 0
CUI: C1832615
Disease: HYPERPARATHYROIDISM, NEONATAL SEVERE
HYPERPARATHYROIDISM, NEONATAL SEVERE 		14 0 1 7.1E-02 0 0
CUI: C0026706
Disease: Mucopolysaccharidosis III
Mucopolysaccharidosis III 		17 0 1 5.9E-02 0 0
CUI: C0221055
Disease: Paramyotonia Congenita (disorder)
Paramyotonia Congenita (disorder) 		17 0 1 5.9E-02 0 0
CUI: C2720163
Disease: Placental Steroid Sulfatase Deficiency
Placental Steroid Sulfatase Deficiency 		17 0 1 5.9E-02 0 0
CUI: C0026697
Disease: Mucolipidoses
Mucolipidoses 		19 0 1 5.3E-02 0 0
CUI: C0086651
Disease: Mucopolysaccharidosis, MPS-IV-A
Mucopolysaccharidosis, MPS-IV-A 		19 0 1 5.3E-02 0 0
CUI: C0086647
Disease: Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type IIIA 		25 0 1 4.0E-02 0 0
CUI: C3150077
Disease: Mild short stature
Mild short stature 		25 0 1 4.0E-02 0 0
CUI: C0026705
Disease: Mucopolysaccharidosis II
Mucopolysaccharidosis II 		26 0 1 3.8E-02 0 0
CUI: C0023522
Disease: Leukodystrophy, Metachromatic
Leukodystrophy, Metachromatic 		27 0 1 3.7E-02 0 0