Source: CLINVAR ×
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: C0027092
Disease: Myopia
Myopia 		45 0 15 5.6E-02 0 0
CUI: C0240635
Disease: Byzanthine arch palate
Byzanthine arch palate 		46 66 15 5.6E-02 1 2.4E-03
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		35 47 14 5.4E-02 3 7.6E-03
CUI: C0028738
Disease: Nystagmus
Nystagmus 		62 83 15 5.3E-02 2 4.6E-03
CUI: C1384666
Disease: hearing impairment
hearing impairment 		88 257 16 5.2E-02 1 1.7E-03
CUI: C0678230
Disease: Congenital Epicanthus
Congenital Epicanthus 		29 30 13 5.1E-02 2 5.3E-03
CUI: C0014877
Disease: Esotropia
Esotropia 		33 0 13 5.1E-02 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		37 49 13 5.0E-02 2 5.0E-03
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		37 0 13 5.0E-02 0 0
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		43 49 13 4.9E-02 2 5.0E-03
CUI: C0232466
Disease: Feeding difficulties
Feeding difficulties 		45 62 13 4.8E-02 1 2.4E-03
CUI: C4317146
Disease: Acid reflux
Acid reflux 		50 0 13 4.7E-02 0 0
CUI: C0278701
Disease: Gastric Adenocarcinoma
Gastric Adenocarcinoma 		30 188 12 4.7E-02 3 5.6E-03
CUI: C4281993
Disease: Neonatal respiratory distress
Neonatal respiratory distress 		31 0 12 4.7E-02 0 0
CUI: C1386048
Disease: Intrauterine retardation
Intrauterine retardation 		41 56 12 4.5E-02 1 2.5E-03
CUI: C1956257
Disease: Pulmonary Stenosis
Pulmonary Stenosis 		19 38 11 4.5E-02 2 5.2E-03
CUI: C0016202
Disease: Flatfoot
Flatfoot 		30 0 11 4.3E-02 0 0
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		30 0 11 4.3E-02 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		31 34 11 4.3E-02 2 5.2E-03
CUI: C0549629
Disease: Abnormal delivery
Abnormal delivery 		32 0 11 4.3E-02 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay 		39 59 11 4.2E-02 1 2.5E-03
CUI: C0086437
Disease: Joint laxity
Joint laxity 		14 0 10 4.1E-02 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears 		17 19 10 4.1E-02 2 5.4E-03
CUI: C1865017
Disease: Thin upper lip vermilion
Thin upper lip vermilion 		18 25 10 4.1E-02 1 2.7E-03
CUI: C1854114
Disease: Short nose
Short nose 		20 23 10 4.0E-02 1 2.7E-03