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: C0426422
Disease: Narrow nose
Narrow nose 		17 0 7 0.18 0 0
CUI: C1856119
Disease: Low hanging columella
Low hanging columella 		17 0 5 0.12 0 0
CUI: C1855722
Disease: Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation
Iris Coloboma with Ptosis, Hypertelorism, and Mental Retardation 		4 0 3 1.0E-01 0 0
CUI: C1867131
Disease: Broad hallux
Broad hallux 		48 14 7 1.0E-01 1 6.7E-02
CUI: C4021254
Disease: Cutaneous finger syndactyly
Cutaneous finger syndactyly 		20 0 4 8.9E-02 0 0
CUI: C0426415
Disease: Large nose
Large nose 		70 0 8 8.8E-02 0 0
CUI: C3697248
Disease: Short lower third of face
Short lower third of face 		33 0 5 8.8E-02 0 0
CUI: C0162285
Disease: Edema of eyelid
Edema of eyelid 		22 0 4 8.5E-02 0 0
CUI: C1853638
Disease: Broad neck
Broad neck 		22 0 4 8.5E-02 0 0
CUI: C0578038
Disease: Thin lips
Thin lips 		99 0 10 8.5E-02 0 0
CUI: C1865992
Disease: Short hallux
Short hallux 		23 0 4 8.3E-02 0 0
CUI: C4025750
Disease: Abnormality of the nasopharynx
Abnormality of the nasopharynx 		10 0 3 8.3E-02 0 0
CUI: C0426891
Disease: Broad thumbs
Broad thumbs 		67 0 7 7.9E-02 0 0
CUI: C1842366
Disease: Low anterior hairline
Low anterior hairline 		71 0 7 7.5E-02 0 0
CUI: C4021343
Disease: Broad hallux phalanx
Broad hallux phalanx 		17 0 3 7.0E-02 0 0
CUI: C4021395
Disease: Abnormality of the antihelix
Abnormality of the antihelix 		17 0 3 7.0E-02 0 0
CUI: C1834055
Disease: Underdeveloped nasal alae
Underdeveloped nasal alae 		79 8 7 6.9E-02 1 0.11
CUI: C1837819
Disease: Cerebrofrontofacial Syndrome
Cerebrofrontofacial Syndrome 		2 0 2 6.9E-02 0 0
CUI: C1849227
Disease: Cleft of chin
Cleft of chin 		2 0 2 6.9E-02 0 0
CUI: C1857761
Disease: Alagille Syndrome 2
Alagille Syndrome 2 		2 0 2 6.9E-02 0 0
CUI: C1863382
Disease: Absent first metatarsal
Absent first metatarsal 		2 0 2 6.9E-02 0 0
CUI: C1863389
Disease: Apert-Crouzon Disease
Apert-Crouzon Disease 		2 0 2 6.9E-02 0 0
CUI: C1956125
Disease: Alagille Syndrome 1
Alagille Syndrome 1 		2 0 2 6.9E-02 0 0
CUI: C2930797
Disease: Hepatic ductular hypoplasia
Hepatic ductular hypoplasia 		2 0 2 6.9E-02 0 0
CUI: C4021360
Disease: Partial duplication of the distal phalanx of the 3rd finger
Partial duplication of the distal phalanx of the 3rd finger 		2 0 2 6.9E-02 0 0