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: C0029294
Disease: Orofaciodigital Syndromes
Orofaciodigital Syndromes
19 0 13 0.57 0 0
CUI: C0431564
Disease: Lobulated tongue
Lobulated tongue
14 0 5 0.19 0 0
CUI: C0431565
Disease: Hamartoma of tongue
Hamartoma of tongue
18 0 5 0.17 0 0
CUI: C4021814
Disease: Accessory oral frenulum
Accessory oral frenulum
12 0 4 0.16 0 0
CUI: C0026363
Disease: Mohr Syndrome
Mohr Syndrome
6 0 3 0.15 0 0
Midline notch of upper alveolar ridge
8 0 3 0.14 0 0
CUI: C1709353
Disease: Osteofibrous Dysplasia
Osteofibrous Dysplasia
25 0 5 0.14 0 0
CUI: C1848595
Disease: Mesoaxial polydactyly
Mesoaxial polydactyly
9 0 3 0.13 0 0
CUI: C1848597
Disease: Central Y-shaped metacarpal
Central Y-shaped metacarpal
9 0 3 0.13 0 0
CUI: C1856655
Disease: Hypoplasia of olfactory tract
Hypoplasia of olfactory tract
9 0 3 0.13 0 0
CUI: C0241438
Disease: Tongue nodules
Tongue nodules
11 0 3 0.12 0 0
CUI: C2931426
Disease: Orofaciodigital syndrome type1
Orofaciodigital syndrome type1
2 0 2 0.12 0 0
CUI: C1865060
Disease: Molar tooth sign on MRI
Molar tooth sign on MRI
35 0 5 0.11 0 0
CUI: C1850256
Disease: Median cleft lip
Median cleft lip
15 0 3 0.10 0 0
Gonadotropin releasing factor deficiency
5 0 2 1.0E-01 0 0
CUI: C0345354
Disease: Radial polydactyly
Radial polydactyly
51 0 6 9.7E-02 0 0
CUI: C0342418
Disease: Hypothalamic hamartomas
Hypothalamic hamartomas
29 0 4 9.5E-02 0 0
CUI: C4024167
Disease: Abnormality of the antitragus
Abnormality of the antitragus
7 0 2 9.1E-02 0 0
CUI: C4025881
Disease: Abnormal oral frenulum morphology
Abnormal oral frenulum morphology
19 0 3 9.1E-02 0 0
CUI: C0238210
Disease: Malrotation of kidney
Malrotation of kidney
8 0 2 8.7E-02 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
61 0 6 8.3E-02 0 0
CUI: C0796147
Disease: Acrocallosal Syndrome
Acrocallosal Syndrome
9 0 2 8.3E-02 0 0
CUI: C0266111
Disease: Bifid tongue
Bifid tongue
24 0 3 7.9E-02 0 0
CUI: C2745997
Disease: OROFACIODIGITAL SYNDROME VI
OROFACIODIGITAL SYNDROME VI
11 0 2 7.7E-02 0 0
CUI: C2748910
Disease: Rett Syndrome, Atypical
Rett Syndrome, Atypical
11 0 2 7.7E-02 0 0