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: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		9 163 5 0.14 1 5.9E-03
CUI: C2718067
Disease: Alcoholic Steatohepatitis
Alcoholic Steatohepatitis 		30 0 7 0.13 0 0
CUI: C0086650
Disease: MPS III D
MPS III D 		4 0 4 0.13 0 0
CUI: C1868556
Disease: Ovoid thoracolumbar vertebrae
Ovoid thoracolumbar vertebrae 		4 0 4 0.13 0 0
CUI: C0086649
Disease: MPS III C
MPS III C 		6 0 4 0.12 0 0
CUI: C0426820
Disease: Thick rib
Thick rib 		6 0 4 0.12 0 0
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		7 0 4 0.12 0 0
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		7 0 4 0.12 0 0
CUI: C1854827
Disease: Heparan sulfate excretion in urine
Heparan sulfate excretion in urine 		7 0 4 0.12 0 0
CUI: C0086648
Disease: MPS III B
MPS III B 		13 0 4 1.0E-01 0 0
CUI: C1854834
Disease: Dense calvaria
Dense calvaria 		3 0 3 9.7E-02 0 0
CUI: C0026706
Disease: Mucopolysaccharidosis III
Mucopolysaccharidosis III 		17 0 4 9.1E-02 0 0
CUI: C0011071
Disease: Sudden death
Sudden death 		30 0 5 8.9E-02 0 0
CUI: C0340375
Disease: Subaortic stenosis
Subaortic stenosis 		19 0 4 8.7E-02 0 0
CUI: C4732796
Disease: Apical hypertrophic cardiomyopathy
Apical hypertrophic cardiomyopathy 		10 0 3 7.9E-02 0 0
CUI: C0005686
Disease: Urinary Bladder Diseases
Urinary Bladder Diseases 		24 0 4 7.8E-02 0 0
CUI: C0086647
Disease: Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type IIIA 		25 0 4 7.7E-02 0 0
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		83 355 8 7.5E-02 4 1.1E-02
CUI: C1846385
Disease: FOCAL CORTICAL DYSPLASIA OF TAYLOR
FOCAL CORTICAL DYSPLASIA OF TAYLOR 		14 0 3 7.1E-02 0 0
CUI: C4025583
Disease: Cellular metachromasia
Cellular metachromasia 		2 0 2 6.5E-02 0 0
CUI: C0581381
Disease: Recurrent upper respiratory tract infection
Recurrent upper respiratory tract infection 		52 0 5 6.4E-02 0 0
CUI: C0086795
Disease: Pfaundler-Hurler Syndrome
Pfaundler-Hurler Syndrome 		36 0 4 6.3E-02 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 24 3 6.1E-02 1 3.3E-02
CUI: C0014236
Disease: Endophthalmitis
Endophthalmitis 		22 0 3 6.0E-02 0 0
CUI: C0232849
Disease: Bladder pain
Bladder pain 		23 0 3 5.9E-02 0 0