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: C1832471
Disease: Renal dysplasia diffuse cystic
Renal dysplasia diffuse cystic 		1 0 1 0.50 0 0
CUI: C1859292
Disease: Triangular-shaped open mouth
Triangular-shaped open mouth 		2 0 1 0.33 0 0
CUI: C3892039
Disease: BARDET-BIEDL SYNDROME 5
BARDET-BIEDL SYNDROME 5 		2 0 1 0.33 0 0
CUI: C4021862
Disease: Absent epiphyses
Absent epiphyses 		2 0 1 0.33 0 0
CUI: C4025010
Disease: Coat hanger sign of ribs
Coat hanger sign of ribs 		2 0 1 0.33 0 0
CUI: C0035637
Disease: Rinderpest
Rinderpest 		3 0 1 0.25 0 0
CUI: C0332154
Disease: Received therapy or drug for
Received therapy or drug for 		3 0 1 0.25 0 0
CUI: C0030846
Disease: Penile Diseases
Penile Diseases 		4 0 1 0.20 0 0
CUI: C1857662
Disease: COACH syndrome
COACH syndrome 		4 0 1 0.20 0 0
CUI: C4020922
Disease: Enlarged fossa interpeduncularis
Enlarged fossa interpeduncularis 		4 0 1 0.20 0 0
CUI: C4025719
Disease: Dysgenesis of the cerebellar vermis
Dysgenesis of the cerebellar vermis 		4 0 1 0.20 0 0
CUI: C0033785
Disease: Pseudarthrosis
Pseudarthrosis 		5 0 1 0.17 0 0
CUI: C0345394
Disease: Hypoplasia of spine
Hypoplasia of spine 		5 0 1 0.17 0 0
CUI: C1836393
Disease: Abnormality of ocular smooth pursuit
Abnormality of ocular smooth pursuit 		5 0 1 0.17 0 0
CUI: C1855677
Disease: Brainstem dysplasia
Brainstem dysplasia 		5 0 1 0.17 0 0
CUI: C3806216
Disease: Neonatal breathing dysregulation
Neonatal breathing dysregulation 		5 0 1 0.17 0 0
CUI: C4274118
Disease: Joubert syndrome with ocular defect
Joubert syndrome with ocular defect 		5 0 1 0.17 0 0
CUI: C3810214
Disease: Elongated superior cerebellar peduncle
Elongated superior cerebellar peduncle 		7 0 1 0.12 0 0
CUI: C0278152
Disease: Hemifacial Spasm
Hemifacial Spasm 		8 0 1 0.11 0 0
CUI: C0015398
Disease: Eye Diseases, Hereditary
Eye Diseases, Hereditary 		9 0 1 1.0E-01 0 0
CUI: C1855284
Disease: Intrahepatic biliary atresia
Intrahepatic biliary atresia 		9 0 1 1.0E-01 0 0
CUI: C0543874
Disease: Apraxia, oculomotor, Cogan type
Apraxia, oculomotor, Cogan type 		10 0 1 9.1E-02 0 0
CUI: C2112942
Disease: Preaxial foot polydactyly
Preaxial foot polydactyly 		10 0 1 9.1E-02 0 0
CUI: C1859846
Disease: Childhood-onset truncal obesity
Childhood-onset truncal obesity 		11 0 1 8.3E-02 0 0
CUI: C0234649
Disease: Abnormal saccadic eye movement
Abnormal saccadic eye movement 		17 0 1 5.6E-02 0 0