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: C0238210
Disease: Malrotation of kidney
Malrotation of kidney 		8 0 2 0.14 0 0
CUI: C0034895
Disease: Rectovaginal Fistula
Rectovaginal Fistula 		17 0 3 0.14 0 0
CUI: C0376524
Disease: Branchio-Oculo-Facial Syndrome
Branchio-Oculo-Facial Syndrome 		9 0 2 0.13 0 0
CUI: C0006131
Disease: Branchioma
Branchioma 		10 0 2 0.12 0 0
CUI: C0079037
Disease: Branchial Clefts-Congenital disorder
Branchial Clefts-Congenital disorder 		1 0 1 0.12 0 0
CUI: C0152415
Disease: Ankyloglossia
Ankyloglossia 		19 0 3 0.12 0 0
CUI: C0238293
Disease: Osteomyelosclerosis
Osteomyelosclerosis 		1 0 1 0.12 0 0
CUI: C0264402
Disease: Gas bubble disease
Gas bubble disease 		1 0 1 0.12 0 0
CUI: C0265241
Disease: Franceschetti-Klein syndrome
Franceschetti-Klein syndrome 		1 0 1 0.12 0 0
CUI: C0456877
Disease: High grade T-cell lymphoma
High grade T-cell lymphoma 		1 0 1 0.12 0 0
CUI: C0543612
Disease: Cervical syndrome
Cervical syndrome 		1 0 1 0.12 0 0
CUI: C1332919
Disease: Cervical Mucinous Adenocarcinoma
Cervical Mucinous Adenocarcinoma 		1 0 1 0.12 0 0
CUI: C1844554
Disease: Absent fingernail
Absent fingernail 		19 0 3 0.12 0 0
CUI: C1854594
Disease: DEAFNESS, AUTOSOMAL DOMINANT 23
DEAFNESS, AUTOSOMAL DOMINANT 23 		1 0 1 0.12 0 0
CUI: C2825742
Disease: Disseminated Juvenile Xanthogranuloma
Disseminated Juvenile Xanthogranuloma 		1 0 1 0.12 0 0
CUI: C3150983
Disease: TREACHER COLLINS SYNDROME 2
TREACHER COLLINS SYNDROME 2 		1 0 1 0.12 0 0
CUI: C4016751
Disease: ANTERIOR SEGMENT ANOMALIES AND CATARACT
ANTERIOR SEGMENT ANOMALIES AND CATARACT 		1 0 1 0.12 0 0
CUI: C4016752
Disease: BRANCHIOOTORENAL SYNDROME WITH CATARACT
BRANCHIOOTORENAL SYNDROME WITH CATARACT 		1 0 1 0.12 0 0
CUI: C4024295
Disease: Hypoplasia of the pharynx
Hypoplasia of the pharynx 		1 0 1 0.12 0 0
CUI: C4025880
Disease: Abnormal parotid gland morphology
Abnormal parotid gland morphology 		1 0 1 0.12 0 0
CUI: C4038750
Disease: RNA polymerase III-related leukodystrophy
RNA polymerase III-related leukodystrophy 		1 0 1 0.12 0 0
CUI: C4225305
Disease: LEUKODYSTROPHY, HYPOMYELINATING, 11
LEUKODYSTROPHY, HYPOMYELINATING, 11 		1 0 1 0.12 0 0
CUI: C0265780
Disease: Congenital absence of lung
Congenital absence of lung 		11 0 2 0.12 0 0
CUI: C1843005
Disease: Absent eyelashes
Absent eyelashes 		21 0 3 0.12 0 0
CUI: C0278076
Disease: Behavioral tic
Behavioral tic 		31 0 4 0.11 0 0