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: C0395971
Disease: Dominant sensorineural hearing loss
Dominant sensorineural hearing loss 		6 0 2 0.17 0 0
CUI: C0240583
Disease: Short upturned nose
Short upturned nose 		1 0 1 0.12 0 0
CUI: C0271574
Disease: Empty Sella Syndrome, Primary
Empty Sella Syndrome, Primary 		1 0 1 0.12 0 0
CUI: C0340535
Disease: Acute massive pulmonary embolism
Acute massive pulmonary embolism 		1 0 1 0.12 0 0
CUI: C0751097
Disease: Empty Sella Syndrome, Secondary
Empty Sella Syndrome, Secondary 		1 0 1 0.12 0 0
CUI: C0948285
Disease: Corneal striae
Corneal striae 		1 0 1 0.12 0 0
CUI: C1858172
Disease: Deafness, Autosomal Dominant 20
Deafness, Autosomal Dominant 20 		1 0 1 0.12 0 0
CUI: C1860752
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 7 		1 0 1 0.12 0 0
CUI: C1865614
Disease: HEMOCHROMATOSIS, TYPE 2A
HEMOCHROMATOSIS, TYPE 2A 		1 0 1 0.12 0 0
CUI: C1970280
Disease: Hearing loss begins with loss of high frequencies
Hearing loss begins with loss of high frequencies 		1 0 1 0.12 0 0
CUI: C1970281
Disease: Audiogram shows sloping configuration
Audiogram shows sloping configuration 		1 0 1 0.12 0 0
CUI: C1970282
Disease: Deafness, profound, by 6th decade
Deafness, profound, by 6th decade 		1 0 1 0.12 0 0
CUI: C1998346
Disease: Autoimmune sensorineural hearing loss
Autoimmune sensorineural hearing loss 		1 0 1 0.12 0 0
CUI: C2363747
Disease: Neurological decompensation
Neurological decompensation 		1 0 1 0.12 0 0
CUI: C2678474
Disease: CARDIOMYOPATHY, DILATED, 2A (disorder)
CARDIOMYOPATHY, DILATED, 2A (disorder) 		1 0 1 0.12 0 0
CUI: C2750091
Disease: Cardiomyopathy, Dilated, 1FF
Cardiomyopathy, Dilated, 1FF 		1 0 1 0.12 0 0
CUI: C3279369
Disease: Microphthalmia (in some patients)
Microphthalmia (in some patients) 		1 0 1 0.12 0 0
CUI: C3280099
Disease: CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME
CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME 		1 0 1 0.12 0 0
CUI: C3281235
Disease: BARAITSER-WINTER SYNDROME 2
BARAITSER-WINTER SYNDROME 2 		1 0 1 0.12 0 0
CUI: C3549665
Disease: Deafness (in some patients)
Deafness (in some patients) 		1 0 1 0.12 0 0
CUI: C3553788
Disease: ALTERNATING HEMIPLEGIA OF CHILDHOOD 2
ALTERNATING HEMIPLEGIA OF CHILDHOOD 2 		1 0 1 0.12 0 0
CUI: C3698167
Disease: Congenital prelingual deafness
Congenital prelingual deafness 		1 0 1 0.12 0 0
CUI: C3808883
Disease: Short neck (in some patients)
Short neck (in some patients) 		1 0 1 0.12 0 0
CUI: C4012410
Disease: Enlarged ventricles (in some patients)
Enlarged ventricles (in some patients) 		1 0 1 0.12 0 0
CUI: C4023332
Disease: Abnormal corneal endothelium morphology
Abnormal corneal endothelium morphology 		1 0 1 0.12 0 0