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: C1864689
Disease: MICROPHTHALMIA, SYNDROMIC 6 (disorder)
MICROPHTHALMIA, SYNDROMIC 6 (disorder) 		1 0 1 1.00 0 0
CUI: C1864825
Disease: Frias syndrome
Frias syndrome 		1 0 1 1.00 0 0
CUI: C2677434
Disease: OROFACIAL CLEFT 11
OROFACIAL CLEFT 11 		1 0 1 1.00 0 0
CUI: C0521706
Disease: Unilateral cataract
Unilateral cataract 		2 0 1 0.50 0 0
CUI: C1335051
Disease: Non-Neoplastic Urinary System Disorder
Non-Neoplastic Urinary System Disorder 		2 0 1 0.50 0 0
CUI: C2014414
Disease: orthopedic disorders
orthopedic disorders 		2 0 1 0.50 0 0
CUI: C0344452
Disease: Microprolactinoma
Microprolactinoma 		3 0 1 0.33 0 0
CUI: C0455792
Disease: Small scrotum
Small scrotum 		3 0 1 0.33 0 0
CUI: C2678503
Disease: AXENFELD-RIEGER SYNDROME, TYPE 3
AXENFELD-RIEGER SYNDROME, TYPE 3 		3 0 1 0.33 0 0
CUI: C0266215
Disease: Anorectal atresia
Anorectal atresia 		4 0 1 0.25 0 0
CUI: C0477984
Disease: Other congenital malformations of anterior segment of eye
Other congenital malformations of anterior segment of eye 		4 0 1 0.25 0 0
CUI: C0423062
Disease: Intermittent divergent squint
Intermittent divergent squint 		5 0 1 0.20 0 0
CUI: C1260894
Disease: Hypertrophic obesity
Hypertrophic obesity 		5 0 1 0.20 0 0
CUI: C1855350
Disease: Inferior vermis hypoplasia
Inferior vermis hypoplasia 		5 0 1 0.20 0 0
CUI: C0345963
Disease: Benign neoplasm of lung
Benign neoplasm of lung 		6 0 1 0.17 0 0
CUI: C0375530
Disease: Congenital Ureteropelvic Junction Obstruction
Congenital Ureteropelvic Junction Obstruction 		6 0 1 0.17 0 0
CUI: C0795693
Disease: Skeletal malformation
Skeletal malformation 		6 0 1 0.17 0 0
CUI: C0795898
Disease: Cleft Palate-Lateral Synechia Syndrome
Cleft Palate-Lateral Synechia Syndrome 		6 0 1 0.17 0 0
CUI: C1856117
Disease: Uplifted earlobe
Uplifted earlobe 		6 0 1 0.17 0 0
CUI: C0018862
Disease: Heberden node
Heberden node 		8 0 1 0.12 0 0
CUI: C0265509
Disease: Congenital anomaly of skeletal bone
Congenital anomaly of skeletal bone 		8 0 1 0.12 0 0
CUI: C0334569
Disease: Odontogenic myxoma
Odontogenic myxoma 		8 0 1 0.12 0 0
CUI: C0344453
Disease: Macroprolactinoma
Macroprolactinoma 		9 0 1 0.11 0 0
CUI: C0457521
Disease: Unicystic ameloblastoma
Unicystic ameloblastoma 		9 0 1 0.11 0 0
CUI: C3550704
Disease: Abnormality of digit
Abnormality of digit 		9 0 1 0.11 0 0