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: C4073184
Disease: Thick hair
Thick hair
16 0 15 0.25 0 0
CUI: C4023385
Disease: Aplasia of the semicircular canal
Aplasia of the semicircular canal
16 0 14 0.23 0 0
CUI: C0855740
Disease: Abnormal platelet function
Abnormal platelet function
21 0 14 0.21 0 0
CUI: C4020962
Disease: Enlarged thorax
Enlarged thorax
25 0 14 0.20 0 0
Noonan syndrome-like disorder with loose anagen hair
19 0 13 0.20 0 0
Aplasia/Hypoplasia of the abdominal wall musculature
32 0 15 0.19 0 0
CUI: C4025749
Disease: Abnormality of the spleen
Abnormality of the spleen
26 0 14 0.19 0 0
Noonan-Like Syndrome With Loose Anagen Hair
22 0 13 0.19 0 0
CUI: C4023397
Disease: Abnormal hair quantity
Abnormal hair quantity
29 0 14 0.19 0 0
CUI: C1275081
Disease: Cardio-facio-cutaneous syndrome
Cardio-facio-cutaneous syndrome
28 0 13 0.17 0 0
CUI: C0238397
Disease: Pulmonary artery stenosis
Pulmonary artery stenosis
36 0 14 0.17 0 0
CUI: C1837732
Disease: Thickened helices
Thickened helices
37 0 14 0.17 0 0
CUI: C0432333
Disease: Abnormal dermatoglyphic pattern
Abnormal dermatoglyphic pattern
44 0 15 0.17 0 0
CUI: C3164374
Disease: Abnormality of pulmonary valve
Abnormality of pulmonary valve
40 0 14 0.16 0 0
CUI: C1855728
Disease: Low posterior hairline
Low posterior hairline
86 0 20 0.16 0 0
CUI: C0206620
Disease: Lymphangioma, Cystic
Lymphangioma, Cystic
43 0 14 0.16 0 0
CUI: C1836940
Disease: Thickened nuchal skin fold
Thickened nuchal skin fold
58 0 16 0.16 0 0
CUI: C1827524
Disease: Wide spaced nipples
Wide spaced nipples
96 0 21 0.16 0 0
CUI: C0024236
Disease: Lymphedema
Lymphedema
61 0 15 0.14 0 0
CUI: C1835884
Disease: Triangular face
Triangular face
111 16 21 0.14 1 5.3E-02
CUI: C0175704
Disease: LEOPARD Syndrome
LEOPARD Syndrome
47 0 13 0.14 0 0
CUI: C0558165
Disease: Curly hair (finding)
Curly hair (finding)
24 0 10 0.14 0 0
CUI: C0587248
Disease: Costello syndrome (disorder)
Costello syndrome (disorder)
50 0 13 0.13 0 0
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis
67 0 15 0.13 0 0
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
59 0 14 0.13 0 0