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: C0020608
Disease: Hypodontia
Hypodontia 		218 0 1 3.3E-03 0 0
CUI: C1387005
Disease: Penis agenesis
Penis agenesis 		217 0 1 3.3E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 3.4E-03 0 0
CUI: C0005612
Disease: Birth Weight
Birth Weight 		214 0 1 3.4E-03 0 0
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		507 0 2 3.4E-03 0 0
CUI: C0239676
Disease: High forehead
High forehead 		211 0 1 3.4E-03 0 0
CUI: C1843367
Disease: Poor school performance
Poor school performance 		211 0 1 3.4E-03 0 0
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		211 0 1 3.4E-03 0 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		208 0 1 3.4E-03 0 0
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria 		199 0 1 3.6E-03 0 0
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease 		186 0 1 3.7E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 3.7E-03 0 0
CUI: C0677936
Disease: Refractory cancer
Refractory cancer 		184 0 1 3.8E-03 0 0
CUI: C1836047
Disease: Long face
Long face 		182 0 1 3.8E-03 0 0
CUI: C0235991
Disease: Small for gestational age (disorder)
Small for gestational age (disorder) 		181 0 1 3.8E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 3.9E-03 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		429 0 2 3.9E-03 0 0
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		173 0 1 3.9E-03 0 0
CUI: C0037763
Disease: Spasm
Spasm 		172 0 1 3.9E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 1 3.9E-03 0 0
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		427 0 2 3.9E-03 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers 		171 0 1 4.0E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement 		169 0 1 4.0E-03 0 0
CUI: C0279068
Disease: Childhood Solid Neoplasm
Childhood Solid Neoplasm 		169 0 1 4.0E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 4.0E-03 0 0