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: C4551560
Disease: Truncal obesity
Truncal obesity 		38 0 1 2.6E-02 0 0
CUI: C0150080
Disease: Social Communication Disorder
Social Communication Disorder 		40 0 1 2.5E-02 0 0
CUI: C0267071
Disease: Oropharyngeal Dysphagia
Oropharyngeal Dysphagia 		43 0 1 2.3E-02 0 0
CUI: C0401149
Disease: Chronic constipation
Chronic constipation 		47 0 1 2.1E-02 0 0
CUI: C1867131
Disease: Broad hallux
Broad hallux 		48 0 1 2.1E-02 0 0
CUI: C1849075
Disease: Relative macrocephaly
Relative macrocephaly 		49 19 1 2.0E-02 1 2.9E-02
CUI: C1865916
Disease: Bilateral ptosis
Bilateral ptosis 		50 0 1 2.0E-02 0 0
CUI: C4317146
Disease: Acid reflux
Acid reflux 		50 58 1 2.0E-02 1 1.4E-02
CUI: C0265535
Disease: Trigonocephaly
Trigonocephaly 		52 0 1 1.9E-02 0 0
CUI: C0581381
Disease: Recurrent upper respiratory tract infection
Recurrent upper respiratory tract infection 		52 0 1 1.9E-02 0 0
CUI: C0020505
Disease: Hyperphagia
Hyperphagia 		60 0 1 1.7E-02 0 0
CUI: C1840069
Disease: Sandal gap
Sandal gap 		62 0 1 1.6E-02 0 0
CUI: C2243051
Disease: Large head (disorder)
Large head (disorder) 		64 116 1 1.6E-02 1 7.6E-03
CUI: C0426891
Disease: Broad thumbs
Broad thumbs 		67 0 1 1.5E-02 0 0
CUI: C0683322
Disease: Mental impairment
Mental impairment 		67 0 1 1.5E-02 0 0
CUI: C0853087
Disease: Nail abnormality
Nail abnormality 		67 0 1 1.5E-02 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		73 14 1 1.4E-02 1 3.4E-02
CUI: C1849340
Disease: Long palpebral fissure
Long palpebral fissure 		73 0 1 1.4E-02 0 0
CUI: C0265529
Disease: Plagiocephaly
Plagiocephaly 		74 0 1 1.4E-02 0 0
CUI: C0015310
Disease: Exotropia
Exotropia 		78 0 1 1.3E-02 0 0
CUI: C0424731
Disease: Single transverse palmar crease
Single transverse palmar crease 		78 0 1 1.3E-02 0 0
CUI: C0752308
Disease: Hypoxia-Ischemia, Brain
Hypoxia-Ischemia, Brain 		81 0 1 1.2E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 1.2E-02 0 0
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele 		85 13 1 1.2E-02 1 3.6E-02
CUI: C1857042
Disease: Sparse scalp hair
Sparse scalp hair 		85 0 1 1.2E-02 0 0