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: C0035508
Disease: Rhonchi
Rhonchi 		2 0 1 5.9E-02 0 0
CUI: C0154286
Disease: Iron deficiency anemia secondary to chronic blood loss
Iron deficiency anemia secondary to chronic blood loss 		2 0 1 5.9E-02 0 0
CUI: C0158621
Disease: Congenital subaortic stenosis
Congenital subaortic stenosis 		2 0 1 5.9E-02 0 0
CUI: C0277827
Disease: Early fontanel closure
Early fontanel closure 		2 0 1 5.9E-02 0 0
CUI: C0433992
Disease: Noise-induced temporary threshold shift
Noise-induced temporary threshold shift 		2 0 1 5.9E-02 0 0
CUI: C1282365
Disease: Mixed type cataract
Mixed type cataract 		2 0 1 5.9E-02 0 0
CUI: C1517444
Disease: Ganglioneuroblastoma, Intermixed
Ganglioneuroblastoma, Intermixed 		2 0 1 5.9E-02 0 0
CUI: C1832334
Disease: CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D
CHARCOT-MARIE-TOOTH DISEASE, TYPE 4D 		2 0 1 5.9E-02 0 0
CUI: C1847827
Disease: LIG4 Syndrome
LIG4 Syndrome 		2 0 1 5.9E-02 0 0
CUI: C1882620
Disease: Rat Cholangiofibrosis
Rat Cholangiofibrosis 		2 0 1 5.9E-02 0 0
CUI: C2030354
Disease: Cardiac Angiosarcoma
Cardiac Angiosarcoma 		2 0 1 5.9E-02 0 0
CUI: C3662490
Disease: Acquired sensorineural hearing loss
Acquired sensorineural hearing loss 		2 0 1 5.9E-02 0 0
CUI: C4024986
Disease: Congenital neuroblastoma
Congenital neuroblastoma 		2 0 1 5.9E-02 0 0
CUI: C4551774
Disease: FEINGOLD SYNDROME 1
FEINGOLD SYNDROME 1 		2 0 1 5.9E-02 0 0
CUI: C4551868
Disease: Stage IIB Cervical Cancer AJCC v6 and v7
Stage IIB Cervical Cancer AJCC v6 and v7 		2 0 1 5.9E-02 0 0
CUI: C4755297
Disease: Somatomammotropinoma
Somatomammotropinoma 		2 0 1 5.9E-02 0 0
CUI: C0238432
Disease: Ependymoma of spinal cord
Ependymoma of spinal cord 		3 0 1 5.6E-02 0 0
CUI: C0278583
Disease: Cervical carcinoma stage IIB
Cervical carcinoma stage IIB 		3 0 1 5.6E-02 0 0
CUI: C0278719
Disease: Extraocular retinoblastoma
Extraocular retinoblastoma 		3 0 1 5.6E-02 0 0
CUI: C0406587
Disease: Wrinkly skin syndrome
Wrinkly skin syndrome 		3 0 1 5.6E-02 0 0
CUI: C1262148
Disease: Grip strength decreased
Grip strength decreased 		3 0 1 5.6E-02 0 0
CUI: C1269700
Disease: Caliectasis
Caliectasis 		3 0 1 5.6E-02 0 0
CUI: C1291317
Disease: Deficiency of transferase
Deficiency of transferase 		3 0 1 5.6E-02 0 0
CUI: C1332215
Disease: Adult Spinal Cord Ependymoma
Adult Spinal Cord Ependymoma 		3 0 1 5.6E-02 0 0
CUI: C1368041
Disease: Pancreatic Somatostatinoma
Pancreatic Somatostatinoma 		3 0 1 5.6E-02 0 0