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: C0278874
Disease: Adult Ependymoma
Adult Ependymoma 		144 0 1 6.9E-03 0 0
CUI: C0796611
Disease: Newly Diagnosed Childhood Ependymoma
Newly Diagnosed Childhood Ependymoma 		144 0 1 6.9E-03 0 0
CUI: C1851584
Disease: Childhood Ependymoma
Childhood Ependymoma 		147 0 1 6.8E-03 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		148 0 1 6.8E-03 0 0
CUI: C0240063
Disease: Coloboma of iris
Coloboma of iris 		153 0 1 6.5E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 5.6E-03 0 0
CUI: C1836047
Disease: Long face
Long face 		182 0 1 5.5E-03 0 0
CUI: C0152427
Disease: Polydactyly
Polydactyly 		188 0 1 5.3E-03 0 0
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II 		194 0 1 5.2E-03 0 0
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria 		199 0 1 5.0E-03 0 0
CUI: C4277690
Disease: Ciliopathies
Ciliopathies 		241 0 1 4.1E-03 0 0
CUI: C0014474
Disease: Ependymoma
Ependymoma 		244 0 1 4.1E-03 0 0
CUI: C0003578
Disease: Apnea
Apnea 		262 0 1 3.8E-03 0 0
CUI: C4551915
Disease: Gait Disturbance, CTCAE
Gait Disturbance, CTCAE 		299 0 1 3.3E-03 0 0
CUI: C2674608
Disease: Feeding difficulties in infancy
Feeding difficulties in infancy 		305 0 1 3.3E-03 0 0
CUI: C0575081
Disease: Gait abnormality
Gait abnormality 		312 0 1 3.2E-03 0 0
CUI: C0019569
Disease: Hirschsprung Disease
Hirschsprung Disease 		384 0 1 2.6E-03 0 0
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		407 0 1 2.5E-03 0 0
CUI: C0009806
Disease: Constipation
Constipation 		424 0 1 2.4E-03 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		473 0 1 2.1E-03 0 0
CUI: C0239234
Disease: Low set ears
Low set ears 		489 0 1 2.0E-03 0 0
CUI: C0011603
Disease: Dermatitis
Dermatitis 		496 0 1 2.0E-03 0 0
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		502 0 1 2.0E-03 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		505 0 1 2.0E-03 0 0
CUI: C0040822
Disease: Tremor
Tremor 		528 0 1 1.9E-03 0 0