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: C1860819
Disease: Metopic synostosis
Metopic synostosis
28 5 21 0.36 1 9.1E-02
CUI: C2931150
Disease: Synostotic Anterior Plagiocephaly
Synostotic Anterior Plagiocephaly
16 0 16 0.31 0 0
CUI: C1833340
Disease: Synostotic Posterior Plagiocephaly
Synostotic Posterior Plagiocephaly
25 0 18 0.31 0 0
CUI: C4551902
Disease: Craniosynostosis, Type 1
Craniosynostosis, Type 1
18 0 16 0.30 0 0
CUI: C0265534
Disease: Scaphycephaly
Scaphycephaly
43 0 21 0.28 0 0
CUI: C0030044
Disease: Acrocephaly
Acrocephaly
35 0 16 0.23 0 0
CUI: C0432123
Disease: Sagittal craniosynostosis
Sagittal craniosynostosis
35 13 14 0.19 1 5.3E-02
CUI: C0039093
Disease: Congenital abnormal Synostosis
Congenital abnormal Synostosis
25 0 9 0.13 0 0
CUI: C0432122
Disease: Interfrontal craniofaciosynostosis
Interfrontal craniofaciosynostosis
7 0 6 0.11 0 0
CUI: C0424711
Disease: Orbital separation diminished
Orbital separation diminished
89 11 14 0.11 2 0.12
CUI: C1856266
Disease: Coronal craniosynostosis
Coronal craniosynostosis
20 0 7 0.11 0 0
CUI: C4021814
Disease: Accessory oral frenulum
Accessory oral frenulum
12 0 6 0.10 0 0
CUI: C0221356
Disease: Brachycephaly
Brachycephaly
186 0 21 9.7E-02 0 0
CUI: C4021343
Disease: Broad hallux phalanx
Broad hallux phalanx
17 0 6 9.5E-02 0 0
CUI: C0423113
Disease: Telecanthus
Telecanthus
134 0 16 9.4E-02 0 0
CUI: C0175699
Disease: Saethre-Chotzen Syndrome
Saethre-Chotzen Syndrome
30 0 7 9.3E-02 0 0
CUI: C0029429
Disease: Osteochondrosis
Osteochondrosis
9 0 5 8.9E-02 0 0
CUI: C1867131
Disease: Broad hallux
Broad hallux
48 14 8 8.7E-02 1 5.0E-02
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly
74 0 10 8.6E-02 0 0
CUI: C1866231
Disease: Full cheeks
Full cheeks
103 4 12 8.4E-02 1 1.0E-01
CUI: C1861869
Disease: Underdeveloped supraorbital ridges
Underdeveloped supraorbital ridges
53 0 8 8.2E-02 0 0
CUI: C0426891
Disease: Broad thumbs
Broad thumbs
67 11 9 8.2E-02 1 5.9E-02
CUI: C0796095
Disease: Opitz trigonocephaly syndrome
Opitz trigonocephaly syndrome
4 0 4 7.7E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome
20 0 5 7.5E-02 0 0
CUI: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis
6 0 4 7.4E-02 0 0