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: C0339693
Disease: Internal Ophthalmoplegia
Internal Ophthalmoplegia 		5 0 1 0.17 0 0
CUI: C1856560
Disease: Bone-marrow foam cells
Bone-marrow foam cells 		5 0 1 0.17 0 0
CUI: C0017083
Disease: Gangliosidoses
Gangliosidoses 		6 0 1 0.14 0 0
CUI: C0267990
Disease: Adult-onset obesity
Adult-onset obesity 		6 0 1 0.14 0 0
CUI: C0696098
Disease: Blood thyroid stimulating hormone analysis
Blood thyroid stimulating hormone analysis 		6 0 1 0.14 0 0
CUI: C1285291
Disease: Fetal ascites
Fetal ascites 		6 0 1 0.14 0 0
CUI: C1320474
Disease: Nuchal Rigidity
Nuchal Rigidity 		6 0 1 0.14 0 0
CUI: C0268242
Disease: Niemann-Pick Disease, Type A
Niemann-Pick Disease, Type A 		7 0 1 0.12 0 0
CUI: C0338473
Disease: Neuroaxonal Dystrophies
Neuroaxonal Dystrophies 		7 0 1 0.12 0 0
CUI: C0348489
Disease: Other sphingolipidosis
Other sphingolipidosis 		7 0 1 0.12 0 0
CUI: C2242456
Disease: thyroid function
thyroid function 		7 0 1 0.12 0 0
CUI: C1843366
Disease: NIEMANN-PICK DISEASE, TYPE C2
NIEMANN-PICK DISEASE, TYPE C2 		9 0 1 1.0E-01 0 0
CUI: C4022417
Disease: Degeneration of the striatum
Degeneration of the striatum 		9 0 1 1.0E-01 0 0
CUI: C0006131
Disease: Branchioma
Branchioma 		10 0 1 9.1E-02 0 0
CUI: C4025651
Disease: Increased circulating cortisol level
Increased circulating cortisol level 		11 0 1 8.3E-02 0 0
CUI: C0750951
Disease: Lenticulostriate Disorders
Lenticulostriate Disorders 		12 0 1 7.7E-02 0 0
CUI: C0242917
Disease: Filoviridae Infections
Filoviridae Infections 		13 0 1 7.1E-02 0 0
CUI: C0278952
Disease: Nasopharyngeal cancer recurrent
Nasopharyngeal cancer recurrent 		13 0 1 7.1E-02 0 0
CUI: C0454596
Disease: Dysarthria, Spastic
Dysarthria, Spastic 		30 0 2 6.7E-02 0 0
CUI: C1845076
Disease: Lymphoproliferative Syndrome, X-Linked, 2
Lymphoproliferative Syndrome, X-Linked, 2 		14 0 1 6.7E-02 0 0
CUI: C0278161
Disease: Ataxia, Motor
Ataxia, Motor 		16 0 1 5.9E-02 0 0
CUI: C0037899
Disease: Sphingolipidoses
Sphingolipidoses 		17 0 1 5.6E-02 0 0
CUI: C0750940
Disease: Tremor, Rubral
Tremor, Rubral 		18 0 1 5.3E-02 0 0
CUI: C0751870
Disease: Heredodegenerative Disorders, Nervous System
Heredodegenerative Disorders, Nervous System 		18 0 1 5.3E-02 0 0
CUI: C1843369
Disease: Vertical supranuclear gaze palsy
Vertical supranuclear gaze palsy 		18 0 1 5.3E-02 0 0