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: C0026363
Disease: Mohr Syndrome
Mohr Syndrome 		6 0 4 0.24 0 0
CUI: C0431565
Disease: Hamartoma of tongue
Hamartoma of tongue 		18 1 5 0.18 1 0.50
CUI: C4021814
Disease: Accessory oral frenulum
Accessory oral frenulum 		12 0 4 0.17 0 0
CUI: C0266111
Disease: Bifid tongue
Bifid tongue 		24 0 5 0.15 0 0
CUI: C0221363
Disease: Bifid nose
Bifid nose 		9 0 3 0.14 0 0
CUI: C1848597
Disease: Central Y-shaped metacarpal
Central Y-shaped metacarpal 		9 0 3 0.14 0 0
CUI: C4025881
Disease: Abnormal oral frenulum morphology
Abnormal oral frenulum morphology 		19 0 4 0.13 0 0
CUI: C0241438
Disease: Tongue nodules
Tongue nodules 		11 0 3 0.13 0 0
CUI: C1850968
Disease: Median cleft palate
Median cleft palate 		3 0 2 0.12 0 0
CUI: C1861373
Disease: Y-shaped metacarpals
Y-shaped metacarpals 		3 0 2 0.12 0 0
CUI: C1969178
Disease: Mesomelic leg shortening
Mesomelic leg shortening 		3 0 2 0.12 0 0
CUI: C1969181
Disease: Aplasia/Hypoplasia of the tibia
Aplasia/Hypoplasia of the tibia 		3 0 2 0.12 0 0
CUI: C4021824
Disease: Postaxial polysyndactyly of foot
Postaxial polysyndactyly of foot 		3 0 2 0.12 0 0
CUI: C0431564
Disease: Lobulated tongue
Lobulated tongue 		14 0 3 0.12 0 0
CUI: C1396772
Disease: Hypoplasia of the epiglottis
Hypoplasia of the epiglottis 		5 0 2 0.11 0 0
CUI: C4021020
Disease: Non-midline cleft lip
Non-midline cleft lip 		16 0 3 0.11 0 0
CUI: C1395852
Disease: Polydactyly preaxial type 1
Polydactyly preaxial type 1 		49 0 6 0.10 0 0
CUI: C1510460
Disease: Orofaciodigital Syndrome I
Orofaciodigital Syndrome I 		17 0 3 0.10 0 0
CUI: C1850259
Disease: Short tibia
Short tibia 		17 0 3 0.10 0 0
CUI: C0266251
Disease: Gallbladder, Agenesis Of
Gallbladder, Agenesis Of 		7 0 2 1.0E-01 0 0
CUI: C0342418
Disease: Hypothalamic hamartomas
Hypothalamic hamartomas 		29 0 4 1.0E-01 0 0
CUI: C0431527
Disease: Laryngeal hypoplasia
Laryngeal hypoplasia 		7 0 2 1.0E-01 0 0
CUI: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes 		19 0 3 9.7E-02 0 0
CUI: C1851853
Disease: Midline notch of upper alveolar ridge
Midline notch of upper alveolar ridge 		8 0 2 9.5E-02 0 0
CUI: C0036996
Disease: Short Rib-Polydactyly Syndrome
Short Rib-Polydactyly Syndrome 		21 0 3 9.1E-02 0 0