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: C1855616
Disease: Cartilaginous ossification of nose
Cartilaginous ossification of nose
1 0 1 0.50 0 0
Premature fusion of phalangeal epiphyses
1 0 1 0.50 0 0
Cartilaginous ossification of larynx
1 0 1 0.50 0 0
Calcification of the auricular cartilage
2 0 1 0.33 0 0
CUI: C1855608
Disease: Costal cartilage calcification
Costal cartilage calcification
2 0 1 0.33 0 0
CUI: C4022015
Disease: Calcification of cartilage
Calcification of cartilage
3 0 1 0.25 0 0
CUI: C0265766
Disease: Congenital atresia of trachea
Congenital atresia of trachea
4 0 1 0.20 0 0
Congenital hypoplasia of pulmonary artery
4 0 1 0.20 0 0
CUI: C1855607
Disease: Keutel syndrome
Keutel syndrome
4 0 1 0.20 0 0
Monckeberg Medial Calcific Sclerosis
5 0 1 0.17 0 0
CUI: C0399451
Disease: Subgingival plaque
Subgingival plaque
9 0 1 1.0E-01 0 0
CUI: C0006666
Disease: Calciphylaxis
Calciphylaxis
10 0 1 9.1E-02 0 0
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin
11 0 1 8.3E-02 0 0
CUI: C4315130
Disease: Hippocampal atrophy
Hippocampal atrophy
13 0 1 7.1E-02 0 0
Small intestinal bacterial overgrowth
14 0 1 6.7E-02 0 0
CUI: C0042880
Disease: Vitamin K Deficiency
Vitamin K Deficiency
19 0 1 5.0E-02 0 0
Peripheral pulmonary artery stenosis
23 0 1 4.2E-02 0 0
CUI: C1865992
Disease: Short hallux
Short hallux
23 0 1 4.2E-02 0 0
CUI: C2316787
Disease: Chronic kidney disease stage 3
Chronic kidney disease stage 3
25 0 1 3.8E-02 0 0
Chronic kidney disease mineral and bone disorder
26 0 1 3.7E-02 0 0
CUI: C1859126
Disease: Stippled epiphyses
Stippled epiphyses
28 0 1 3.4E-02 0 0
CUI: C0741796
Disease: Recurrent bronchitis
Recurrent bronchitis
29 0 1 3.3E-02 0 0
CUI: C0920296
Disease: Developmental reading disorder
Developmental reading disorder
33 0 1 2.9E-02 0 0
CUI: C0238397
Disease: Pulmonary artery stenosis
Pulmonary artery stenosis
36 0 1 2.7E-02 0 0
CUI: C0473583
Disease: Nevus elasticus
Nevus elasticus
37 0 1 2.6E-02 0 0