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: C0042485
Disease: Venous Insufficiency
Venous Insufficiency 		0 1 0 0 1 1.1E-02
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia 		0 1 0 0 1 1.1E-02
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		0 1 0 0 1 1.1E-02
CUI: C0394006
Disease: Dysequilibrium syndrome
Dysequilibrium syndrome 		0 1 0 0 1 1.1E-02
CUI: C0549117
Disease: Frontal lobe syndrome
Frontal lobe syndrome 		0 3 0 0 3 3.2E-02
CUI: C0751771
Disease: Sleep Bruxism
Sleep Bruxism 		0 4 0 0 1 1.0E-02
CUI: C0878520
Disease: beta Thalassemia, heterozygous
beta Thalassemia, heterozygous 		0 2 0 0 2 2.1E-02
CUI: C1262483
Disease: Hereditary stomatocytosis
Hereditary stomatocytosis 		0 2 0 0 1 1.0E-02
CUI: C1855995
Disease: L-2-HYDROXYGLUTARIC ACIDURIA
L-2-HYDROXYGLUTARIC ACIDURIA 		0 16 0 0 1 9.1E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 1.1E-02
CUI: C2746066
Disease: Combined D-2- and L-2-hydroxyglutaric aciduria
Combined D-2- and L-2-hydroxyglutaric aciduria 		0 14 0 0 1 9.3E-03
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 2.2E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 2.3E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 2.5E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		137 0 1 2.5E-03 0 0
CUI: C0423113
Disease: Telecanthus
Telecanthus 		134 0 1 2.5E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color 		130 0 1 2.6E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 2.6E-03 0 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet 		129 0 1 2.6E-03 0 0
CUI: C1328407
Disease: Hip Dysplasia
Hip Dysplasia 		128 0 1 2.6E-03 0 0
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly 		123 0 1 2.6E-03 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes 		121 0 1 2.6E-03 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly 		120 0 1 2.6E-03 0 0
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle 		118 0 1 2.7E-03 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge 		117 0 1 2.7E-03 0 0