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: C0840564
Disease: Rupture of bladder
Rupture of bladder 		1 0 1 0.25 0 0
CUI: C1303076
Disease: Tortuous carotid artery
Tortuous carotid artery 		1 0 1 0.25 0 0
CUI: C1836050
Disease: Filaminopathy, autosomal dominant
Filaminopathy, autosomal dominant 		1 0 1 0.25 0 0
CUI: C1836336
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4H 		1 8 1 0.25 2 0.25
CUI: C1862133
Disease: Decreased finger mobility
Decreased finger mobility 		1 0 1 0.25 0 0
CUI: C1866805
Disease: Unilateral narrow palpebral fissure
Unilateral narrow palpebral fissure 		1 0 1 0.25 0 0
CUI: C3276032
Disease: Hypoplastic areola
Hypoplastic areola 		1 0 1 0.25 0 0
CUI: C3279722
Disease: MYOPATHY, DISTAL, 4
MYOPATHY, DISTAL, 4 		1 0 1 0.25 0 0
CUI: C4022453
Disease: Abnormal morphology of ulna
Abnormal morphology of ulna 		1 0 1 0.25 0 0
CUI: C4310748
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 5
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 5 		1 0 1 0.25 0 0
CUI: C4310749
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26 		1 0 1 0.25 0 0
CUI: C4310784
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 41
MENTAL RETARDATION, AUTOSOMAL DOMINANT 41 		1 0 1 0.25 0 0
CUI: C4476982
Disease: Two-raphe bicuspid aortic valve
Two-raphe bicuspid aortic valve 		1 0 1 0.25 0 0
CUI: C4531288
Disease: Abnormal morphology of left ventricular trabeculae
Abnormal morphology of left ventricular trabeculae 		1 0 1 0.25 0 0
CUI: C1141933
Disease: Multi-organ disorder
Multi-organ disorder 		2 0 1 0.20 0 0
CUI: C1839512
Disease: Limited knee flexion
Limited knee flexion 		2 0 1 0.20 0 0
CUI: C1845359
Disease: Spinal Muscular Atrophy, Distal, X-Linked 3
Spinal Muscular Atrophy, Distal, X-Linked 3 		2 0 1 0.20 0 0
CUI: C1865644
Disease: Plantar Lipomatosis, Unusual Facies, and Developmental Delay
Plantar Lipomatosis, Unusual Facies, and Developmental Delay 		2 0 1 0.20 0 0
CUI: C4021264
Disease: Abnormal ventricular septum morphology
Abnormal ventricular septum morphology 		2 0 1 0.20 0 0
CUI: C4022157
Disease: Muscle fiber cytoplasmatic inclusion bodies
Muscle fiber cytoplasmatic inclusion bodies 		2 0 1 0.20 0 0
CUI: C4025031
Disease: Aplasia/hypoplasia of the humerus
Aplasia/hypoplasia of the humerus 		2 0 1 0.20 0 0
CUI: C4025537
Disease: Humerus varus
Humerus varus 		2 0 1 0.20 0 0
CUI: C4477022
Disease: Finger flexor weakness
Finger flexor weakness 		2 0 1 0.20 0 0
CUI: C0340429
Disease: Familial restrictive cardiomyopathy (disorder)
Familial restrictive cardiomyopathy (disorder) 		3 0 1 0.17 0 0
CUI: C0685201
Disease: Hemangioma of spleen
Hemangioma of spleen 		3 0 1 0.17 0 0