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: C0003910
Disease: Articulation Disorders
Articulation Disorders 		1 0 1 7.5E-03 0 0
CUI: C0006262
Disease: Bronchial Fistula
Bronchial Fistula 		1 0 1 7.5E-03 0 0
CUI: C0015338
Disease: Exstrophy
Exstrophy 		1 0 1 7.5E-03 0 0
CUI: C0023441
Disease: Leukemia, Experimental
Leukemia, Experimental 		1 0 1 7.5E-03 0 0
CUI: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms 		1 0 1 7.5E-03 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 7.5E-03 0 0
CUI: C0153470
Disease: Malignant neoplasm of spleen
Malignant neoplasm of spleen 		1 0 1 7.5E-03 0 0
CUI: C0158564
Disease: Congenital vitreous anomaly
Congenital vitreous anomaly 		1 0 1 7.5E-03 0 0
CUI: C0158667
Disease: Aplasia of Lacrimal and Salivary Glands
Aplasia of Lacrimal and Salivary Glands 		1 0 1 7.5E-03 0 0
CUI: C0158763
Disease: Macrodactylia of fingers
Macrodactylia of fingers 		1 0 1 7.5E-03 0 0
CUI: C0158768
Disease: Macrodactyly of toe
Macrodactyly of toe 		1 0 1 7.5E-03 0 0
CUI: C0158784
Disease: Accessory skeletal muscle
Accessory skeletal muscle 		1 0 1 7.5E-03 0 0
CUI: C0231246
Disease: Failure to gain weight
Failure to gain weight 		1 0 1 7.5E-03 0 0
CUI: C0232180
Disease: Cardiac shunt
Cardiac shunt 		1 0 1 7.5E-03 0 0
CUI: C0233286
Disease: Frank Breech Presentation
Frank Breech Presentation 		1 0 1 7.5E-03 0 0
CUI: C0233623
Disease: Onychotillomania
Onychotillomania 		1 0 1 7.5E-03 0 0
CUI: C0238415
Disease: SCLERODERMA, PULMONARY
SCLERODERMA, PULMONARY 		1 0 1 7.5E-03 0 0
CUI: C0243057
Disease: Stomatognathic System Abnormalities
Stomatognathic System Abnormalities 		1 0 1 7.5E-03 0 0
CUI: C0264558
Disease: Tension Pneumothorax
Tension Pneumothorax 		1 0 1 7.5E-03 0 0
CUI: C0265248
Disease: Ruvalcaba Syndrome
Ruvalcaba Syndrome 		1 0 1 7.5E-03 0 0
CUI: C0265809
Disease: Double outlet left ventricle
Double outlet left ventricle 		1 0 1 7.5E-03 0 0
CUI: C0265843
Disease: Congenital atresia of aortic valve
Congenital atresia of aortic valve 		1 0 1 7.5E-03 0 0
CUI: C0266878
Disease: External resorption of tooth
External resorption of tooth 		1 0 1 7.5E-03 0 0
CUI: C0268357
Disease: Osteogenesis imperfecta, type 1A
Osteogenesis imperfecta, type 1A 		1 0 1 7.5E-03 0 0
CUI: C0271616
Disease: Precocious female puberty
Precocious female puberty 		1 1 1 7.5E-03 1 7.7E-02