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: C0086650
Disease: MPS III D
MPS III D 		4 0 4 0.57 0 0
CUI: C1868556
Disease: Ovoid thoracolumbar vertebrae
Ovoid thoracolumbar vertebrae 		4 0 4 0.57 0 0
CUI: C0086649
Disease: MPS III C
MPS III C 		6 0 4 0.44 0 0
CUI: C0426820
Disease: Thick rib
Thick rib 		6 0 4 0.44 0 0
CUI: C1854834
Disease: Dense calvaria
Dense calvaria 		3 0 3 0.43 0 0
CUI: C4025583
Disease: Cellular metachromasia
Cellular metachromasia 		2 0 2 0.29 0 0
CUI: C0026706
Disease: Mucopolysaccharidosis III
Mucopolysaccharidosis III 		17 0 5 0.26 0 0
CUI: C0086648
Disease: MPS III B
MPS III B 		13 0 4 0.25 0 0
CUI: C1854774
Disease: Dermatan sulfate excretion in urine
Dermatan sulfate excretion in urine 		3 0 2 0.25 0 0
CUI: C0086647
Disease: Mucopolysaccharidosis Type IIIA
Mucopolysaccharidosis Type IIIA 		25 0 5 0.19 0 0
CUI: C0086795
Disease: Pfaundler-Hurler Syndrome
Pfaundler-Hurler Syndrome 		36 0 6 0.16 0 0
CUI: C4024726
Disease: Mucopolysacchariduria
Mucopolysacchariduria 		8 0 2 0.15 0 0
CUI: C0026703
Disease: Mucopolysaccharidoses
Mucopolysaccharidoses 		48 0 7 0.15 0 0
CUI: C0266062
Disease: Posterior open bite
Posterior open bite 		1 0 1 0.14 0 0
CUI: C0342841
Disease: Hunter's syndrome, severe form
Hunter's syndrome, severe form 		1 0 1 0.14 0 0
CUI: C0342842
Disease: Hunter's syndrome, mild form
Hunter's syndrome, mild form 		1 0 1 0.14 0 0
CUI: C0795821
Disease: Chromosome 7, trisomy 7q
Chromosome 7, trisomy 7q 		1 0 1 0.14 0 0
CUI: C1854749
Disease: Proximal tapering of metacarpals
Proximal tapering of metacarpals 		1 0 1 0.14 0 0
CUI: C2718304
Disease: Sulfoiduronate Sulfatase Deficiency
Sulfoiduronate Sulfatase Deficiency 		1 0 1 0.14 0 0
CUI: C4023599
Disease: Abnormality of carbohydrate metabolism/homeostasis
Abnormality of carbohydrate metabolism/homeostasis 		1 0 1 0.14 0 0
CUI: C4025306
Disease: Anterior beaking of lower thoracic vertebrae
Anterior beaking of lower thoracic vertebrae 		1 0 1 0.14 0 0
CUI: C4225287
Disease: RETINITIS PIGMENTOSA 73
RETINITIS PIGMENTOSA 73 		1 0 1 0.14 0 0
CUI: C4225306
Disease: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2V 		1 0 1 0.14 0 0
CUI: C4552512
Disease: Neurocognitive deficit
Neurocognitive deficit 		1 0 1 0.14 0 0
CUI: C0270707
Disease: Kluver-Bucy Syndrome
Kluver-Bucy Syndrome 		10 0 2 0.13 0 0