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: C4274084
Disease: Pelizaeus Merzbacher like disease
Pelizaeus Merzbacher like disease 		10 0 5 0.16 0 0
CUI: C1864723
Disease: Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency
Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 		5 0 4 0.14 0 0
CUI: C0270733
Disease: Striatonigral Degeneration
Striatonigral Degeneration 		7 0 4 0.13 0 0
CUI: C0020501
Disease: Primary Hyperoxaluria
Primary Hyperoxaluria 		16 11 5 0.13 5 2.9E-02
CUI: C1839264
Disease: SPASTIC PARAPLEGIA 2, X-LINKED (disorder)
SPASTIC PARAPLEGIA 2, X-LINKED (disorder) 		8 0 4 0.13 0 0
CUI: C0751604
Disease: Hereditary X-Linked Recessive Spastic Paraplegia
Hereditary X-Linked Recessive Spastic Paraplegia 		10 0 4 0.12 0 0
CUI: C0020500
Disease: Hyperoxaluria
Hyperoxaluria 		49 3 8 0.12 1 5.8E-03
CUI: C0443306
Disease: Spastic
Spastic 		13 0 4 0.11 0 0
CUI: C0795953
Disease: MASA SYNDROME (disorder)
MASA SYNDROME (disorder) 		16 0 4 0.10 0 0
CUI: C0451718
Disease: Non-obstructive reflux-associated chronic pyelonephritis (disorder)
Non-obstructive reflux-associated chronic pyelonephritis (disorder) 		13 0 3 8.1E-02 0 0
CUI: C3495566
Disease: Reflux nephropathy (disorder)
Reflux nephropathy (disorder) 		13 0 3 8.1E-02 0 0
CUI: C0020630
Disease: Hypophosphatasia
Hypophosphatasia 		27 0 4 8.0E-02 0 0
CUI: C1849156
Disease: Spastic Ataxia
Spastic Ataxia 		28 0 4 7.8E-02 0 0
CUI: C0205711
Disease: Pelizaeus-Merzbacher Disease
Pelizaeus-Merzbacher Disease 		30 0 4 7.5E-02 0 0
CUI: C0277525
Disease: Infectious gastroenteritis
Infectious gastroenteritis 		2 0 2 7.4E-02 0 0
CUI: C3824909
Disease: Arthritis in animals
Arthritis in animals 		2 0 2 7.4E-02 0 0
CUI: C2677109
Disease: Leukodystrophy, Hypomyelinating, 4
Leukodystrophy, Hypomyelinating, 4 		3 0 2 7.1E-02 0 0
CUI: C1334414
Disease: Barretts esophagus with low grade dysplasia
Barretts esophagus with low grade dysplasia 		4 0 2 6.9E-02 0 0
CUI: C0332983
Disease: Malassez' epithelial rests
Malassez' epithelial rests 		6 0 2 6.5E-02 0 0
CUI: C0266313
Disease: Allanson Pantzar McLeod syndrome
Allanson Pantzar McLeod syndrome 		8 0 2 6.1E-02 0 0
CUI: C0022681
Disease: Medullary sponge kidney
Medullary sponge kidney 		9 0 2 5.9E-02 0 0
CUI: C0268397
Disease: Amyloidosis, Primary Cutaneous
Amyloidosis, Primary Cutaneous 		9 0 2 5.9E-02 0 0
CUI: C0520739
Disease: Hereditary pyropoikilocytosis
Hereditary pyropoikilocytosis 		47 0 4 5.7E-02 0 0
CUI: C1740787
Disease: Cardiac autonomic neuropathy
Cardiac autonomic neuropathy 		11 0 2 5.6E-02 0 0
CUI: C0156259
Disease: Hypertrophy of kidney
Hypertrophy of kidney 		31 0 3 5.5E-02 0 0