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: C1840238
Disease: Midnasal stenosis
Midnasal stenosis 		16 0 16 0.20 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		18 0 16 0.20 0 0
CUI: C1840235
Disease: SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR 		20 0 16 0.19 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 25 42 0.19 1 3.1E-02
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		22 0 16 0.19 0 0
CUI: C4551564
Disease: Narrow nasal bridge
Narrow nasal bridge 		47 0 19 0.18 0 0
CUI: C0266174
Disease: Duodenal atresia
Duodenal atresia 		36 0 17 0.17 0 0
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		39 0 16 0.16 0 0
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly 		51 0 17 0.15 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 25 0.15 0 0
CUI: C1854114
Disease: Short nose
Short nose 		265 0 44 0.15 0 0
CUI: C0018916
Disease: Hemangioma
Hemangioma 		69 0 17 0.13 0 0
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding) 		96 0 20 0.13 0 0
CUI: C0424711
Disease: Orbital separation diminished
Orbital separation diminished 		89 11 18 0.12 1 5.6E-02
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		82 0 17 0.12 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		97 0 17 0.11 0 0
CUI: C4023180
Disease: Type 1 muscle fiber atrophy
Type 1 muscle fiber atrophy 		15 0 9 0.11 0 0
CUI: C0399526
Disease: Class III malocclusion
Class III malocclusion 		147 0 21 0.10 0 0
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure 		73 0 14 0.10 0 0
CUI: C0151526
Disease: Premature Birth
Premature Birth 		163 50 22 1.0E-01 1 1.8E-02
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		100 0 16 9.8E-02 0 0
CUI: C0019553
Disease: Hip Contracture
Hip Contracture 		33 0 10 9.8E-02 0 0
CUI: C0039685
Disease: Tetralogy of Fallot
Tetralogy of Fallot 		146 0 20 9.8E-02 0 0
CUI: C0424688
Disease: Small head
Small head 		11 0 8 9.8E-02 0 0
CUI: C1845447
Disease: Cupped ears (finding)
Cupped ears (finding) 		45 0 11 9.7E-02 0 0