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: C4025749
Disease: Abnormality of the spleen
Abnormality of the spleen
26 0 8 0.13 0 0
CUI: C1842870
Disease: Chromosome 1p36 Deletion Syndrome
Chromosome 1p36 Deletion Syndrome
6 0 5 0.12 0 0
CUI: C0158465
Disease: Acquired cubitus valgus
Acquired cubitus valgus
35 0 8 0.12 0 0
CUI: C0265695
Disease: Congenital fusion of ribs
Congenital fusion of ribs
37 0 8 0.11 0 0
CUI: C0576093
Disease: Knee joint valgus deformity
Knee joint valgus deformity
117 0 16 0.11 0 0
CUI: C1857002
Disease: Capitate-hamate fusion
Capitate-hamate fusion
8 0 5 0.11 0 0
CUI: C4024996
Disease: Aplasia/Hypoplasia of the lungs
Aplasia/Hypoplasia of the lungs
29 0 7 0.11 0 0
CUI: C4721788
Disease: Bifid ribs
Bifid ribs
9 0 5 0.11 0 0
CUI: C1458140
Disease: Bleeding tendency
Bleeding tendency
71 0 11 0.11 0 0
CUI: C0856748
Disease: Aneurysm of aortic arch
Aneurysm of aortic arch
20 0 6 0.11 0 0
CUI: C0277828
Disease: Late fontanel closure
Late fontanel closure
41 0 8 0.11 0 0
CUI: C3277019
Disease: Horizontal eyebrow
Horizontal eyebrow
11 0 5 0.10 0 0
CUI: C1846439
Disease: Hypoplasia of the odontoid process
Hypoplasia of the odontoid process
23 0 6 0.10 0 0
CUI: C1865992
Disease: Short hallux
Short hallux
23 0 6 0.10 0 0
CUI: C0034194
Disease: Pyloric Stenosis
Pyloric Stenosis
121 0 15 0.10 0 0
CUI: C0018920
Disease: Hemangioma, Cavernous
Hemangioma, Cavernous
36 0 7 9.9E-02 0 0
CUI: C0086795
Disease: Pfaundler-Hurler Syndrome
Pfaundler-Hurler Syndrome
36 0 7 9.9E-02 0 0
CUI: C1855665
Disease: Ovoid vertebral bodies
Ovoid vertebral bodies
25 0 6 9.8E-02 0 0
CUI: C0266623
Disease: Congenital anomaly of neck
Congenital anomaly of neck
26 0 6 9.7E-02 0 0
Abnormality of female external genitalia
15 0 5 9.6E-02 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes
61 0 9 9.6E-02 0 0
CUI: C0023221
Disease: Leg Length Inequality
Leg Length Inequality
27 0 6 9.5E-02 0 0
CUI: C4025329
Disease: Abnormality of the anus
Abnormality of the anus
16 0 5 9.4E-02 0 0
CUI: C4023397
Disease: Abnormal hair quantity
Abnormal hair quantity
29 0 6 9.2E-02 0 0
Myopathy, Centronuclear, Autosomal Recessive
6 0 4 9.1E-02 0 0