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: C0233689
Disease: Delusion of infidelity
Delusion of infidelity 		0 1 0 0 1 0.12
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 1 1.0E-01
CUI: C1963757
Disease: Dopamine dysregulation syndrome
Dopamine dysregulation syndrome 		0 1 0 0 1 0.12
CUI: C2677565
Disease: AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder) 		0 25 0 0 1 3.1E-02
CUI: C3148872
Disease: FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED 		0 3 0 0 1 1.0E-01
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge 		180 0 1 1.8E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia 		169 0 1 1.8E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control 		162 0 1 1.8E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 1.8E-03 0 0
CUI: C1855285
Disease: Protruding ear
Protruding ear 		152 0 1 1.8E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 1.9E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		142 0 1 1.9E-03 0 0
CUI: C1837397
Disease: Severe global developmental delay
Severe global developmental delay 		130 0 1 1.9E-03 0 0
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios 		129 0 1 1.9E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause 		129 0 1 1.9E-03 0 0
CUI: C0746674
Disease: Generalized muscle weakness
Generalized muscle weakness 		126 0 1 1.9E-03 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose 		123 0 1 1.9E-03 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes 		121 0 1 2.0E-03 0 0
CUI: C4552811
Disease: Generalized Muscle Weakness, CTCAE
Generalized Muscle Weakness, CTCAE 		117 0 1 2.0E-03 0 0
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		116 0 1 2.0E-03 0 0
CUI: C1837770
Disease: Sparse hair
Sparse hair 		112 0 1 2.0E-03 0 0
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder) 		109 0 1 2.0E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 2.0E-03 0 0
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome 		105 0 1 2.0E-03 0 0
CUI: C1853487
Disease: Thick eyebrow
Thick eyebrow 		104 0 1 2.0E-03 0 0