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: C0030625
Disease: Passive Cutaneous Anaphylaxis
Passive Cutaneous Anaphylaxis 		1 0 1 0.17 0 0
CUI: C0265201
Disease: De Sanctis-Cacchione syndrome
De Sanctis-Cacchione syndrome 		1 0 1 0.17 0 0
CUI: C0344688
Disease: Patent Ductus Venosus
Patent Ductus Venosus 		1 0 1 0.17 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF 		1 0 1 0.17 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF 		1 0 1 0.17 0 0
CUI: C1832253
Disease: INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF
INTIMAL MEDIAL THICKNESS OF INTERNAL CAROTID ARTERY, MODIFIER OF 		1 0 1 0.17 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1 		1 0 1 0.17 0 0
CUI: C1837756
Disease: MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY
MANDIBULOACRAL DYSPLASIA WITH TYPE B LIPODYSTROPHY 		1 0 1 0.17 0 0
CUI: C1837781
Disease: Increased subcutaneous truncal adipose tissue
Increased subcutaneous truncal adipose tissue 		1 0 1 0.17 0 0
CUI: C1851430
Disease: Subcortical white matter calcifications
Subcortical white matter calcifications 		1 0 1 0.17 0 0
CUI: C1851431
Disease: Cerebellar calcifications
Cerebellar calcifications 		1 0 1 0.17 0 0
CUI: C1857652
Disease: Thymic hormone decreased
Thymic hormone decreased 		1 0 1 0.17 0 0
CUI: C1859224
Disease: Second metatarsal posteriorly placed
Second metatarsal posteriorly placed 		1 0 1 0.17 0 0
CUI: C1861693
Disease: Cervical Vertebral Dysplasia
Cervical Vertebral Dysplasia 		1 0 1 0.17 0 0
CUI: C3151063
Disease: MACULAR DEGENERATION, AGE-RELATED, 5
MACULAR DEGENERATION, AGE-RELATED, 5 		1 0 1 0.17 0 0
CUI: C3279800
Disease: KEPPEN-LUBINSKY SYNDROME
KEPPEN-LUBINSKY SYNDROME 		1 0 1 0.17 0 0
CUI: C3502054
Disease: Leukodystrophy, Dysmyelinating, with Oligodontia
Leukodystrophy, Dysmyelinating, with Oligodontia 		1 0 1 0.17 0 0
CUI: C3551173
Disease: UV-SENSITIVE SYNDROME 1
UV-SENSITIVE SYNDROME 1 		1 0 1 0.17 0 0
CUI: C3553298
Disease: UV-SENSITIVE SYNDROME 2
UV-SENSITIVE SYNDROME 2 		1 0 1 0.17 0 0
CUI: C4016735
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF 		1 0 1 0.17 0 0
CUI: C4022977
Disease: Increased carotid artery intimal medial thickness
Increased carotid artery intimal medial thickness 		1 0 1 0.17 0 0
CUI: C4024826
Disease: Pigmentation anomalies of sun-exposed skin
Pigmentation anomalies of sun-exposed skin 		1 0 1 0.17 0 0
CUI: C4025617
Disease: Atlantoaxial abnormality
Atlantoaxial abnormality 		1 0 1 0.17 0 0
CUI: C4310783
Disease: PREMATURE OVARIAN FAILURE 11
PREMATURE OVARIAN FAILURE 11 		1 0 1 0.17 0 0
CUI: C0024689
Disease: Mandibular Diseases
Mandibular Diseases 		2 0 1 0.14 0 0