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: C0393907
Disease: Axonal sensorimotor neuropathy
Axonal sensorimotor neuropathy 		9 0 1 1.0E-01 0 0
CUI: C1720775
Disease: Renal tubular necrosis
Renal tubular necrosis 		9 0 1 1.0E-01 0 0
CUI: C0426428
Disease: Bifid nasal tip
Bifid nasal tip 		10 0 1 9.1E-02 0 0
CUI: C1834954
Disease: Coronal cleft vertebrae
Coronal cleft vertebrae 		11 0 1 8.3E-02 0 0
CUI: C3887547
Disease: Central sleep apnea syndrome
Central sleep apnea syndrome 		11 0 1 8.3E-02 0 0
CUI: C0393574
Disease: Huntington Disease, Late Onset
Huntington Disease, Late Onset 		12 0 1 7.7E-02 0 0
CUI: C0751207
Disease: Akinetic-Rigid Variant of Huntington Disease
Akinetic-Rigid Variant of Huntington Disease 		12 0 1 7.7E-02 0 0
CUI: C0751208
Disease: Juvenile Huntington Disease
Juvenile Huntington Disease 		12 0 1 7.7E-02 0 0
CUI: C1833308
Disease: NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE V 		12 0 1 7.7E-02 0 0
CUI: C2931276
Disease: Spastic paraplegia 17
Spastic paraplegia 17 		12 0 1 7.7E-02 0 0
CUI: C1833561
Disease: UV-Sensitive Syndrome
UV-Sensitive Syndrome 		15 0 1 6.2E-02 0 0
CUI: C1865384
Disease: Amyotrophy, monomelic
Amyotrophy, monomelic 		15 0 1 6.2E-02 0 0
CUI: C0008039
Disease: Cheyne-Stokes Respiration
Cheyne-Stokes Respiration 		16 0 1 5.9E-02 0 0
CUI: C0393541
Disease: Distal Spinal Muscular Atrophy
Distal Spinal Muscular Atrophy 		16 0 1 5.9E-02 0 0
CUI: C1866021
Disease: Increased connective tissue
Increased connective tissue 		16 0 1 5.9E-02 0 0
CUI: C0339546
Disease: Retinal Pigment Epithelial Detachment
Retinal Pigment Epithelial Detachment 		17 0 1 5.6E-02 0 0
CUI: C4520981
Disease: Abnormality of the basal ganglia
Abnormality of the basal ganglia 		17 0 1 5.6E-02 0 0
CUI: C4739246
Disease: Apnea+hypopnea
Apnea+hypopnea 		17 0 1 5.6E-02 0 0
CUI: C0432211
Disease: Spondyloepimetaphyseal disorder
Spondyloepimetaphyseal disorder 		37 0 2 5.4E-02 0 0
CUI: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve 		18 0 1 5.3E-02 0 0
CUI: C0949856
Disease: Oxidative Phosphorylation Deficiencies
Oxidative Phosphorylation Deficiencies 		18 0 1 5.3E-02 0 0
CUI: C4021761
Disease: Morphological abnormality of the pyramidal tract
Morphological abnormality of the pyramidal tract 		18 0 1 5.3E-02 0 0
CUI: C0265290
Disease: Metaphyseal chondrodysplasia
Metaphyseal chondrodysplasia 		20 0 1 4.8E-02 0 0
CUI: C0239548
Disease: Fasciculation, Tongue
Fasciculation, Tongue 		21 0 1 4.5E-02 0 0
CUI: C0002896
Disease: Sideroblastic anemia
Sideroblastic anemia 		22 0 1 4.3E-02 0 0