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: C0020619
Disease: Hypogonadism
Hypogonadism 		305 0 1 2.3E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		255 0 1 2.6E-03 0 0
CUI: C0004509
Disease: Azoospermia
Azoospermia 		254 0 1 2.6E-03 0 0
CUI: C0456070
Disease: Growth delay
Growth delay 		244 0 1 2.6E-03 0 0
CUI: C4277690
Disease: Ciliopathies
Ciliopathies 		241 0 1 2.6E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.7E-03 0 0
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		219 0 1 2.8E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 1 2.8E-03 0 0
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders 		218 0 1 2.8E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		215 0 1 2.8E-03 0 0
CUI: C0039273
Disease: Talipes cavus
Talipes cavus 		213 0 1 2.9E-03 0 0
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		208 0 1 2.9E-03 0 0
CUI: C0029422
Disease: Osteochondrodysplasias
Osteochondrodysplasias 		207 0 1 2.9E-03 0 0
CUI: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia 		197 0 1 3.0E-03 0 0
CUI: C0034012
Disease: Delayed Puberty
Delayed Puberty 		196 0 1 3.0E-03 0 0
CUI: C0023520
Disease: Leukodystrophy
Leukodystrophy 		190 0 1 3.1E-03 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly 		186 0 1 3.1E-03 0 0
CUI: C0410528
Disease: Skeletal dysplasia
Skeletal dysplasia 		186 0 1 3.1E-03 0 0
CUI: C0205647
Disease: Follicular adenoma
Follicular adenoma 		183 0 1 3.1E-03 0 0
CUI: C0015469
Disease: Facial paralysis
Facial paralysis 		182 0 1 3.1E-03 0 0
CUI: C0399526
Disease: Class III malocclusion
Class III malocclusion 		181 0 1 3.1E-03 0 0
CUI: C1837249
Disease: Malformations of Cortical Development, Group II
Malformations of Cortical Development, Group II 		180 0 1 3.2E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 1 3.2E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		172 0 1 3.2E-03 0 0
CUI: C0027868
Disease: Neuromuscular Diseases
Neuromuscular Diseases 		171 0 1 3.2E-03 0 0