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: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		389 50 61 9.5E-02 1 1.4E-02
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		148 0 40 9.5E-02 0 0
CUI: C0036572
Disease: Seizures
Seizures 		2152 553 213 9.5E-02 2 3.5E-03
CUI: C0542476
Disease: Forgetful
Forgetful 		429 0 64 9.5E-02 0 0
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria 		199 0 44 9.4E-02 0 0
CUI: C1854418
Disease: Biparietal narrowing
Biparietal narrowing 		60 0 32 9.4E-02 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		473 0 67 9.3E-02 0 0
CUI: C0029422
Disease: Osteochondrodysplasias
Osteochondrodysplasias 		207 0 44 9.3E-02 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		217 0 44 9.1E-02 0 0
CUI: C0029124
Disease: Optic Atrophy
Optic Atrophy 		568 0 73 9.0E-02 0 0
CUI: C0239234
Disease: Low set ears
Low set ears 		489 64 66 9.0E-02 1 1.2E-02
CUI: C4049796
Disease: Abnormality of cardiovascular system morphology
Abnormality of cardiovascular system morphology 		198 0 42 9.0E-02 0 0
CUI: C4551583
Disease: Cerebral cortical atrophy
Cerebral cortical atrophy 		271 13 48 9.0E-02 1 2.9E-02
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
Sensorineural Hearing Loss (disorder) 		783 0 90 9.0E-02 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE 		175 0 40 8.9E-02 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption 		175 3 40 8.9E-02 1 4.0E-02
CUI: C0003578
Disease: Apnea
Apnea 		262 0 47 8.9E-02 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 28 8.9E-02 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 93 37 8.8E-02 2 1.8E-02
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 33 8.8E-02 0 0
CUI: C0030486
Disease: Paraplegia
Paraplegia 		59 0 30 8.8E-02 0 0
CUI: C0333068
Disease: Flexion contracture
Flexion contracture 		210 32 42 8.7E-02 2 3.8E-02
CUI: C0410528
Disease: Skeletal dysplasia
Skeletal dysplasia 		186 0 40 8.7E-02 0 0
CUI: C0086543
Disease: Cataract
Cataract 		878 0 95 8.7E-02 0 0
CUI: C1854301
Disease: Motor delay
Motor delay 		384 34 55 8.6E-02 2 3.6E-02