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: C0267952
Disease: Fibrosis of pancreas
Fibrosis of pancreas 		72 0 15 0.15 0 0
CUI: C0014065
Disease: Congenital cerebral hernia
Congenital cerebral hernia 		93 0 17 0.14 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		80 0 15 0.14 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		148 0 23 0.14 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 18 0.14 0 0
CUI: C0431904
Disease: Ulnar polydactyly of fingers
Ulnar polydactyly of fingers 		92 0 16 0.14 0 0
CUI: C0240063
Disease: Coloboma of iris
Coloboma of iris 		153 0 23 0.13 0 0
CUI: C1843496
Disease: Bilateral microphthalmos
Bilateral microphthalmos 		35 11 9 0.13 1 7.7E-02
CUI: C1855675
Disease: Arima syndrome
Arima syndrome 		11 0 6 0.13 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 8 0.12 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 16 0.12 0 0
CUI: C1854418
Disease: Biparietal narrowing
Biparietal narrowing 		60 0 11 0.12 0 0
CUI: C4025819
Disease: Abnormality of the hypothalamus-pituitary axis
Abnormality of the hypothalamus-pituitary axis 		70 0 12 0.12 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge 		117 0 17 0.12 0 0
CUI: C3714581
Disease: Multicystic Dysplastic Kidney
Multicystic Dysplastic Kidney 		121 0 17 0.12 0 0
CUI: C1866231
Disease: Full cheeks
Full cheeks 		103 0 15 0.12 0 0
CUI: C4551568
Disease: Joubert syndrome 1
Joubert syndrome 1 		26 0 7 0.11 0 0
CUI: C0079924
Disease: Oligohydramnios
Oligohydramnios 		129 0 17 0.11 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes 		61 0 10 0.11 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		137 0 17 0.10 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 13 0.10 0 0
CUI: C0158733
Disease: Hand polydactyly
Hand polydactyly 		75 0 11 0.10 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia 		100 0 13 0.10 0 0
CUI: C0240896
Disease: Fundus coloboma
Fundus coloboma 		57 0 9 1.0E-01 0 0
CUI: C3540764
Disease: Coloboma of the Retina
Coloboma of the Retina 		58 0 9 9.9E-02 0 0