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: C1275100
Disease: Keratoderma with deafness
Keratoderma with deafness 		1 0 1 0.12 0 0
CUI: C1611171
Disease: Thalamic infarction
Thalamic infarction 		1 0 1 0.12 0 0
CUI: C1832250
Disease: OBESITY, MODIFIER OF
OBESITY, MODIFIER OF 		1 0 1 0.12 0 0
CUI: C1832251
Disease: BODY MASS INDEX, MODIFIER OF
BODY MASS INDEX, MODIFIER OF 		1 0 1 0.12 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 0.12 0 0
CUI: C1836302
Disease: Carotid Intimal Medial Thickness 1
Carotid Intimal Medial Thickness 1 		1 0 1 0.12 0 0
CUI: C1845576
Disease: Unilateral chest hypoplasia
Unilateral chest hypoplasia 		1 0 1 0.12 0 0
CUI: C1853104
Disease: ALOPECIA AREATA 2
ALOPECIA AREATA 2 		1 0 1 0.12 0 0
CUI: C1865234
Disease: ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS
ICHTHYOSIS, HYSTRIX-LIKE, WITH DEAFNESS 		1 0 1 0.12 0 0
CUI: C1868414
Disease: HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO
HYPERAPOBETALIPOPROTEINEMIA, SUSCEPTIBILITY TO 		1 0 1 0.12 0 0
CUI: C2315694
Disease: Bilateral sensory hearing loss
Bilateral sensory hearing loss 		1 0 1 0.12 0 0
CUI: C2675750
Disease: DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 3A (disorder) 		1 0 1 0.12 0 0
CUI: C2748531
Disease: Perifollicular fibrosis
Perifollicular fibrosis 		1 0 1 0.12 0 0
CUI: C2930930
Disease: Abdominal obesity metabolic syndrome
Abdominal obesity metabolic syndrome 		10 0 2 0.12 0 0
CUI: C3502469
Disease: Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And Kidney Dysplasia-Hypoplasia 		1 0 1 0.12 0 0
CUI: C3806745
Disease: PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED
PALMOPLANTAR KERATODERMA, MUTILATING, WITH PERIORIFICIAL KERATOTIC PLAQUES, X-LINKED 		1 0 1 0.12 0 0
CUI: C3863587
Disease: enterovirus d68 infection
enterovirus d68 infection 		1 0 1 0.12 0 0
CUI: C4016470
Disease: IFAP SYNDROME
IFAP SYNDROME 		1 0 1 0.12 0 0
CUI: C4016735
Disease: DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF
DIABETES MELLITUS, NONINSULIN-DEPENDENT, MODIFIER OF 		1 0 1 0.12 0 0
CUI: C4022977
Disease: Increased carotid artery intimal medial thickness
Increased carotid artery intimal medial thickness 		1 0 1 0.12 0 0
CUI: C4023328
Disease: Abnormality of corneal stroma
Abnormality of corneal stroma 		1 0 1 0.12 0 0
CUI: C4746956
Disease: OSTEOGENESIS IMPERFECTA, TYPE XIX
OSTEOGENESIS IMPERFECTA, TYPE XIX 		1 0 1 0.12 0 0
CUI: C0027424
Disease: Nasal congestion (finding)
Nasal congestion (finding) 		2 0 1 0.11 0 0
CUI: C0240444
Disease: Pachyonychia
Pachyonychia 		2 0 1 0.11 0 0
CUI: C0263221
Disease: Acute eczema
Acute eczema 		2 0 1 0.11 0 0