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: C0026244
Disease: Mitochondrial Swelling
Mitochondrial Swelling 		1 0 1 0.25 0 0
CUI: C0345218
Disease: Low anorectal malformation
Low anorectal malformation 		1 0 1 0.25 0 0
CUI: C2749019
Disease: JOUBERT SYNDROME 10 (disorder)
JOUBERT SYNDROME 10 (disorder) 		1 0 1 0.25 0 0
CUI: C3280556
Disease: PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS
PERIPHERAL NEUROPATHY, MYOPATHY, HOARSENESS, AND HEARING LOSS 		1 0 1 0.25 0 0
CUI: C4748684
Disease: MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC
MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC 		1 0 1 0.25 0 0
CUI: C0265251
Disease: Oto-Palato-digital syndrome type 1
Oto-Palato-digital syndrome type 1 		2 0 1 0.20 0 0
CUI: C1419610
Disease: RP23 gene
RP23 gene 		2 0 1 0.20 0 0
CUI: C1833503
Disease: Deafness, Autosomal Dominant 4
Deafness, Autosomal Dominant 4 		2 0 1 0.20 0 0
CUI: C1846175
Disease: SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder)
SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 2 (disorder) 		2 0 1 0.20 0 0
CUI: C1858545
Disease: Facial capillary hemangioma
Facial capillary hemangioma 		2 0 1 0.20 0 0
CUI: C2931426
Disease: Orofaciodigital syndrome type1
Orofaciodigital syndrome type1 		2 0 1 0.20 0 0
CUI: C0035637
Disease: Rinderpest
Rinderpest 		3 0 1 0.17 0 0
CUI: C0332154
Disease: Received therapy or drug for
Received therapy or drug for 		3 0 1 0.17 0 0
CUI: C2931015
Disease: Dandy Walker variant
Dandy Walker variant 		3 0 1 0.17 0 0
CUI: C1865598
Disease: Alveolar ridge overgrowth
Alveolar ridge overgrowth 		5 0 1 0.12 0 0
CUI: C4023965
Disease: Structural foot deformity
Structural foot deformity 		5 0 1 0.12 0 0
CUI: C0026363
Disease: Mohr Syndrome
Mohr Syndrome 		6 0 1 0.11 0 0
CUI: C0202455
Disease: Platinum measurement
Platinum measurement 		6 0 1 0.11 0 0
CUI: C0848765
Disease: Hearing disability
Hearing disability 		6 0 1 0.11 0 0
CUI: C1856202
Disease: U-Shaped upper lip vermilion
U-Shaped upper lip vermilion 		6 0 1 0.11 0 0
CUI: C2674738
Disease: Abnormality of toe
Abnormality of toe 		6 0 1 0.11 0 0
CUI: C0029166
Disease: Oral Manifestations
Oral Manifestations 		7 0 1 1.0E-01 0 0
CUI: C0269209
Disease: Hydrometrocolpos
Hydrometrocolpos 		7 0 1 1.0E-01 0 0
CUI: C0854078
Disease: Diabetic end stage renal disease
Diabetic end stage renal disease 		7 0 1 1.0E-01 0 0
CUI: C1842160
Disease: MYOPATHY, MYOSIN STORAGE (disorder)
MYOPATHY, MYOSIN STORAGE (disorder) 		7 0 1 1.0E-01 0 0