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: C1839829
Disease: Short distal phalanx of finger
Short distal phalanx of finger
85 0 13 8.2E-02 0 0
Abnormality of cardiovascular system morphology
198 13 21 8.0E-02 1 7.7E-02
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide
429 0 38 7.9E-02 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features
194 0 20 7.7E-02 0 0
CUI: C0239137
Disease: Coxa valga
Coxa valga
68 0 11 7.6E-02 0 0
Flexion contracture of proximal interphalangeal joint
168 0 18 7.6E-02 0 0
CUI: C1853242
Disease: Midface retrusion
Midface retrusion
228 0 22 7.5E-02 0 0
CUI: C0795690
Disease: Congenital omphalocele
Congenital omphalocele
85 0 12 7.5E-02 0 0
Abnormality of immune system physiology
42 0 9 7.5E-02 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead
159 0 17 7.4E-02 0 0
CUI: C1839739
Disease: Thick lower lip vermilion
Thick lower lip vermilion
145 0 16 7.4E-02 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia
191 0 19 7.3E-02 0 0
CUI: C4025790
Disease: Specific learning disability
Specific learning disability
165 0 17 7.2E-02 0 0
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril
407 0 33 7.2E-02 0 0
Aplasia/Hypoplasia of the corpus callosum
108 0 13 7.1E-02 0 0
CUI: C0221355
Disease: Macrocephaly
Macrocephaly
367 0 30 7.1E-02 0 0
CUI: C0340375
Disease: Subaortic stenosis
Subaortic stenosis
19 0 7 7.1E-02 0 0
CUI: C0239234
Disease: Low set ears
Low set ears
489 0 38 7.1E-02 0 0
CUI: C0431447
Disease: Synophrys
Synophrys
111 0 13 7.0E-02 0 0
CUI: C0221357
Disease: Brachydactyly
Brachydactyly
325 0 27 7.0E-02 0 0
CUI: C0266231
Disease: Ectopic anus
Ectopic anus
20 0 7 7.0E-02 0 0
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
253 0 22 6.9E-02 0 0
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal
225 0 20 6.8E-02 0 0
CUI: C0423867
Disease: Fine hair
Fine hair
69 0 10 6.8E-02 0 0
CUI: C0576226
Disease: Short foot
Short foot
116 0 13 6.8E-02 0 0