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: C0265931
Disease: Persistent left superior vena cava
Persistent left superior vena cava
2 0 1 0.33 0 0
CUI: C1859477
Disease: Hypoplasia of proximal radius
Hypoplasia of proximal radius
2 0 1 0.33 0 0
CUI: C4025716
Disease: Abnormality of the duodenum
Abnormality of the duodenum
2 0 1 0.33 0 0
CUI: C1260327
Disease: Langerhans Cell Sarcoma
Langerhans Cell Sarcoma
5 0 1 0.17 0 0
CUI: C1865598
Disease: Alveolar ridge overgrowth
Alveolar ridge overgrowth
5 0 1 0.17 0 0
CUI: C0334587
Disease: Astroblastoma
Astroblastoma
6 0 1 0.14 0 0
CUI: C1845272
Disease: Prominent antihelix
Prominent antihelix
6 0 1 0.14 0 0
CUI: C0270742
Disease: Athetoid cerebral palsy
Athetoid cerebral palsy
8 0 1 0.11 0 0
CUI: C0162442
Disease: Parapsoriasis en Plaques
Parapsoriasis en Plaques
9 0 1 1.0E-01 0 0
CUI: C0575497
Disease: Short sternum
Short sternum
9 0 1 1.0E-01 0 0
CUI: C0241438
Disease: Tongue nodules
Tongue nodules
11 0 1 8.3E-02 0 0
Greig cephalopolysyndactyly syndrome
14 0 1 6.7E-02 0 0
CUI: C4023721
Disease: Abnormal hair pattern
Abnormal hair pattern
15 0 1 6.2E-02 0 0
Extramedullary Hematopoiesis Function
16 0 1 5.9E-02 0 0
CUI: C1842680
Disease: Small earlobe
Small earlobe
17 0 1 5.6E-02 0 0
Widely patent fontanelles and sutures
17 0 1 5.6E-02 0 0
CUI: C1861921
Disease: Cutaneous syndactyly
Cutaneous syndactyly
17 0 1 5.6E-02 0 0
CUI: C0031900
Disease: Pierre Robin Syndrome
Pierre Robin Syndrome
39 0 2 5.1E-02 0 0
CUI: C0745287
Disease: infertility tubal factor
infertility tubal factor
19 0 1 5.0E-02 0 0
CUI: C1302772
Disease: Primary cutaneous lymphoma
Primary cutaneous lymphoma
19 0 1 5.0E-02 0 0
CUI: C1857539
Disease: Deep palmar crease
Deep palmar crease
23 0 1 4.2E-02 0 0
CUI: C0267048
Disease: Glossoptosis
Glossoptosis
25 0 1 3.8E-02 0 0
CUI: C1276146
Disease: Cutaneous lymphoma
Cutaneous lymphoma
36 0 1 2.7E-02 0 0
CUI: C0685381
Disease: Congenital hypoplasia of radius
Congenital hypoplasia of radius
37 0 1 2.6E-02 0 0
CUI: C0175701
Disease: Aarskog syndrome
Aarskog syndrome
42 0 1 2.3E-02 0 0