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: C1840235
Disease: SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR
SOLITARY MEDIAN MAXILLARY CENTRAL INCISOR 		20 0 18 0.20 0 0
CUI: C1840238
Disease: Midnasal stenosis
Midnasal stenosis 		16 0 16 0.18 0 0
CUI: C0751617
Disease: Semilobar Holoprosencephaly
Semilobar Holoprosencephaly 		17 0 16 0.18 0 0
CUI: C0266174
Disease: Duodenal atresia
Duodenal atresia 		39 0 19 0.17 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly 		37 2 18 0.17 1 8.3E-02
CUI: C4551564
Disease: Narrow nasal bridge
Narrow nasal bridge 		47 0 19 0.16 0 0
CUI: C0266667
Disease: Cyclocephaly
Cyclocephaly 		35 0 17 0.16 0 0
CUI: C0431363
Disease: Alobar Holoprosencephaly
Alobar Holoprosencephaly 		16 0 14 0.15 0 0
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 25 34 0.14 2 5.9E-02
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		104 7 23 0.14 1 5.9E-02
CUI: C0079541
Disease: Holoprosencephaly
Holoprosencephaly 		109 0 23 0.13 0 0
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		73 0 18 0.12 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 22 0.12 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 8 18 0.12 1 5.6E-02
CUI: C0151526
Disease: Premature Birth
Premature Birth 		192 50 28 0.11 1 1.7E-02
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		52 7 14 0.11 2 0.12
CUI: C2936786
Disease: Aqueductal Stenosis
Aqueductal Stenosis 		34 0 12 0.11 0 0
CUI: C4021395
Disease: Abnormality of the antihelix
Abnormality of the antihelix 		17 0 10 0.10 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		109 0 18 1.0E-01 0 0
CUI: C1843496
Disease: Bilateral microphthalmos
Bilateral microphthalmos 		35 0 11 9.7E-02 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities 		115 0 18 9.7E-02 0 0
CUI: C1860819
Disease: Metopic synostosis
Metopic synostosis 		28 5 10 9.3E-02 1 6.7E-02
CUI: C4023616
Disease: Abnormality of immune system physiology
Abnormality of immune system physiology 		42 0 11 9.2E-02 0 0
CUI: C1854114
Disease: Short nose
Short nose 		265 0 29 8.9E-02 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		148 0 19 8.7E-02 0 0