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: C0456097
Disease: Congenital viral disease
Congenital viral disease 		1 0 1 0.25 0 0
CUI: C1850407
Disease: Navajo Familial Neurogenic Arthropathy
Navajo Familial Neurogenic Arthropathy 		1 0 1 0.25 0 0
CUI: C2242708
Disease: Hypertransaminasaemia
Hypertransaminasaemia 		1 1 1 0.25 1 1.00
CUI: C3151513
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 3 (HEPATOCEREBRAL TYPE) 		1 0 1 0.25 0 0
CUI: C3280721
Disease: CHILBLAIN LUPUS 2
CHILBLAIN LUPUS 2 		1 0 1 0.25 0 0
CUI: C4025018
Disease: Depletion of mitochondrial DNA in liver
Depletion of mitochondrial DNA in liver 		1 0 1 0.25 0 0
CUI: C4025595
Disease: Viral infection-induced rhabdomyolysis
Viral infection-induced rhabdomyolysis 		1 0 1 0.25 0 0
CUI: C4310690
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE)
MITOCHONDRIAL DNA DEPLETION SYNDROME 15 (HEPATOCEREBRAL TYPE) 		1 0 1 0.25 0 0
CUI: C4310733
Disease: PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 4 		1 0 1 0.25 0 0
CUI: C4310935
Disease: MITOCHONDRIAL DNA DEPLETION SYNDROME 3
MITOCHONDRIAL DNA DEPLETION SYNDROME 3 		1 0 1 0.25 0 0
CUI: C0220993
Disease: Cystathioninuria
Cystathioninuria 		2 0 1 0.20 0 0
CUI: C1856979
Disease: Deep white matter hypodensities
Deep white matter hypodensities 		2 0 1 0.20 0 0
CUI: C2749659
Disease: AICARDI-GOUTIERES SYNDROME 5 (disorder)
AICARDI-GOUTIERES SYNDROME 5 (disorder) 		2 0 1 0.20 0 0
CUI: C4024920
Disease: Decreased distal sensory nerve action potential
Decreased distal sensory nerve action potential 		2 0 1 0.20 0 0
CUI: C4310735
Disease: PORTAL HYPERTENSION, NONCIRRHOTIC
PORTAL HYPERTENSION, NONCIRRHOTIC 		2 0 1 0.20 0 0
CUI: C1864975
Disease: Osteomyelitis leading to amputation due to slow healing fractures
Osteomyelitis leading to amputation due to slow healing fractures 		3 0 1 0.17 0 0
CUI: C1865361
Disease: SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES
SHORT STATURE, AUDITORY CANAL ATRESIA, MANDIBULAR HYPOPLASIA, SKELETAL ABNORMALITIES 		3 0 1 0.17 0 0
CUI: C2931254
Disease: Alport syndrome, recessive type
Alport syndrome, recessive type 		3 0 1 0.17 0 0
CUI: C1850415
Disease: Microvesicular hepatic steatosis
Microvesicular hepatic steatosis 		11 0 2 0.15 0 0
CUI: C0010398
Disease: Cruveilhier-Baumgarten Syndrome
Cruveilhier-Baumgarten Syndrome 		4 0 1 0.14 0 0
CUI: C1328348
Disease: Mitochondrial hepatopathy
Mitochondrial hepatopathy 		4 0 1 0.14 0 0
CUI: C1849766
Disease: Periportal fibrosis
Periportal fibrosis 		4 0 1 0.14 0 0
CUI: C1850406
Disease: NAVAJO NEUROHEPATOPATHY
NAVAJO NEUROHEPATOPATHY 		4 0 1 0.14 0 0
CUI: C1850413
Disease: Reye syndrome-like episodes
Reye syndrome-like episodes 		4 0 1 0.14 0 0
CUI: C1855652
Disease: Fetus Small for Gestational Age
Fetus Small for Gestational Age 		4 2 1 0.14 1 0.50