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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 3.8E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 5.6E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 9.5E-02
CUI: C1281440
Disease: Familial obesity
Familial obesity 		0 3 0 0 1 5.0E-02
CUI: C2937224
Disease: Constitutional obesity
Constitutional obesity 		0 3 0 0 1 5.0E-02
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 5.6E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 5.0E-02
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		417 0 1 1.8E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.6E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		211 0 1 2.8E-03 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		208 0 1 2.8E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech 		208 0 1 2.8E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 0 1 2.9E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia 		191 0 1 2.9E-03 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly 		188 0 1 3.0E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 3 3.0E-03 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 3.0E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 3.0E-03 0 0
CUI: C0026034
Disease: Microstomia
Microstomia 		172 0 1 3.1E-03 0 0
CUI: C0423224
Disease: Sunken eyes
Sunken eyes 		171 0 1 3.1E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 3.1E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 3.2E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 3.2E-03 0 0
CUI: C4025790
Disease: Specific learning disability
Specific learning disability 		165 0 1 3.2E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 3.2E-03 0 0