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: C4225278
Disease: GLIOMA SUSCEPTIBILITY 9
GLIOMA SUSCEPTIBILITY 9 		1 0 1 6.2E-02 0 0
CUI: C4225288
Disease: SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION
SHORT STATURE, MICROCEPHALY, AND ENDOCRINE DYSFUNCTION 		1 0 1 6.2E-02 0 0
CUI: C4280757
Disease: Fast-growing nails
Fast-growing nails 		1 0 1 6.2E-02 0 0
CUI: C4546640
Disease: Hypertrichosis cubiti short stature
Hypertrichosis cubiti short stature 		1 0 1 6.2E-02 0 0
CUI: C4553413
Disease: Stage IIB Cervical Cancer AJCC v8
Stage IIB Cervical Cancer AJCC v8 		1 0 1 6.2E-02 0 0
CUI: C4725876
Disease: Resectable Neuroblastoma
Resectable Neuroblastoma 		1 0 1 6.2E-02 0 0
CUI: C4725878
Disease: Unresectable Neuroblastoma
Unresectable Neuroblastoma 		1 0 1 6.2E-02 0 0
CUI: C0153405
Disease: Malignant neoplasm of pharynx
Malignant neoplasm of pharynx 		37 0 3 6.0E-02 0 0
CUI: C0032230
Disease: Pleural Rub
Pleural Rub 		2 0 1 5.9E-02 0 0
CUI: C0035234
Disease: Respiratory Sounds
Respiratory Sounds 		2 0 1 5.9E-02 0 0
CUI: C0035508
Disease: Rhonchi
Rhonchi 		2 0 1 5.9E-02 0 0
CUI: C0036646
Disease: Age-related cataract
Age-related cataract 		92 0 6 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: C0348801
Disease: Group B streptococcal pneumonia
Group B streptococcal pneumonia 		20 0 2 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: C1846950
Disease: Short middle phalanx of finger
Short middle phalanx of finger 		20 0 2 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