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: C0221356
Disease: Brachycephaly
Brachycephaly
186 0 16 8.5E-02 0 0
CUI: C0220767
Disease: Craniofrontonasal dysplasia
Craniofrontonasal dysplasia
8 0 2 8.3E-02 0 0
CUI: C2242703
Disease: Cardio-Renal Syndrome
Cardio-Renal Syndrome
21 0 3 8.3E-02 0 0
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly
74 0 7 8.2E-02 0 0
CUI: C1867131
Disease: Broad hallux
Broad hallux
48 0 5 8.2E-02 0 0
CUI: C0029429
Disease: Osteochondrosis
Osteochondrosis
9 0 2 8.0E-02 0 0
CUI: C0221363
Disease: Bifid nose
Bifid nose
9 0 2 8.0E-02 0 0
CUI: C1853486
Disease: Widow's peak
Widow's peak
9 0 2 8.0E-02 0 0
CUI: C1857484
Disease: Brachyturricephaly
Brachyturricephaly
9 0 2 8.0E-02 0 0
CUI: C1865992
Disease: Short hallux
Short hallux
23 0 3 7.9E-02 0 0
Abnormal nasolacrimal system morphology
23 0 3 7.9E-02 0 0
CUI: C0423823
Disease: Thin nails
Thin nails
10 0 2 7.7E-02 0 0
CUI: C0432235
Disease: CRANIOECTODERMAL DYSPLASIA 1
CRANIOECTODERMAL DYSPLASIA 1
10 0 2 7.7E-02 0 0
CUI: C2930865
Disease: Ramer Ladda syndrome
Ramer Ladda syndrome
10 0 2 7.7E-02 0 0
CUI: C4025750
Disease: Abnormality of the nasopharynx
Abnormality of the nasopharynx
10 0 2 7.7E-02 0 0
CUI: C1853737
Disease: Prominent occiput
Prominent occiput
53 0 5 7.6E-02 0 0
CUI: C1857485
Disease: Flat forehead
Flat forehead
11 0 2 7.4E-02 0 0
CUI: C4021787
Disease: Abnormal diaphysis morphology
Abnormal diaphysis morphology
11 0 2 7.4E-02 0 0
CUI: C4551571
Disease: Cranioectodermal dysplasia
Cranioectodermal dysplasia
11 0 2 7.4E-02 0 0
CUI: C0151740
Disease: Intracranial Hypertension
Intracranial Hypertension
72 0 6 7.1E-02 0 0
CUI: C1281931
Disease: Obstruction of nasolacrimal duct
Obstruction of nasolacrimal duct
12 0 2 7.1E-02 0 0
CUI: C4021161
Disease: Multiple suture craniosynostosis
Multiple suture craniosynostosis
12 0 2 7.1E-02 0 0
CUI: C0010273
Disease: Craniofacial Dysostosis
Craniofacial Dysostosis
14 0 2 6.7E-02 0 0
CUI: C0584837
Disease: Choanal stenosis
Choanal stenosis
14 0 2 6.7E-02 0 0
CUI: C0410529
Disease: Hypochondroplasia (disorder)
Hypochondroplasia (disorder)
16 0 2 6.2E-02 0 0