Source: INFERRED ×
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: C0266174
Disease: Duodenal atresia
Duodenal atresia 		36 0 23 0.36 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		18 0 18 0.35 0 0
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		22 0 19 0.35 0 0
CUI: C1840238
Disease: Midnasal stenosis
Midnasal stenosis 		16 0 16 0.31 0 0
CUI: C1840235
Disease: SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR 		20 0 16 0.29 0 0
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		39 0 19 0.27 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		82 0 24 0.22 0 0
CUI: C1859692
Disease: Decreased cervical spine mobility
Decreased cervical spine mobility 		12 0 11 0.21 0 0
CUI: C4551564
Disease: Narrow nasal bridge
Narrow nasal bridge 		47 0 16 0.20 0 0
CUI: C3279222
Disease: Aplasia/Hypoplasia of the cerebellum
Aplasia/Hypoplasia of the cerebellum 		116 0 26 0.18 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		97 0 22 0.17 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		144 0 28 0.17 0 0
CUI: C0424711
Disease: Orbital separation diminished
Orbital separation diminished 		89 0 20 0.17 0 0
CUI: C0240063
Disease: Coloboma of iris
Coloboma of iris 		146 0 28 0.17 0 0
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		100 0 21 0.16 0 0
CUI: C2750604
Disease: Median cleft lip and palate
Median cleft lip and palate 		15 0 9 0.16 0 0
CUI: C0018916
Disease: Hemangioma
Hemangioma 		69 0 16 0.15 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 0 17 0.15 0 0
CUI: C0010964
Disease: Dandy-Walker Syndrome
Dandy-Walker Syndrome 		111 0 21 0.15 0 0
CUI: C0338503
Disease: Septo-Optic Dysplasia
Septo-Optic Dysplasia 		19 0 9 0.15 0 0
CUI: C0175754
Disease: Agenesis of corpus callosum
Agenesis of corpus callosum 		216 0 34 0.15 0 0
CUI: C0338502
Disease: Hypoplasia of the optic nerve
Hypoplasia of the optic nerve 		54 0 13 0.14 0 0
CUI: C0431376
Disease: Cobblestone Lissencephaly
Cobblestone Lissencephaly 		15 0 8 0.14 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 20 0.14 0 0
CUI: C3279571
Disease: Ectopic posterior pituitary
Ectopic posterior pituitary 		16 2 8 0.14 1 2.6E-02