Source: ALL
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: C0003076
Disease: Aniridia
Aniridia 		0 29 0 0 1 8.4E-03
CUI: C0344542
Disease: Aniridia type 1
Aniridia type 1 		0 87 0 0 1 5.6E-03
CUI: C4310809
Disease: ANTERIOR SEGMENT DYSGENESIS 5
ANTERIOR SEGMENT DYSGENESIS 5 		0 32 0 0 1 8.2E-03
CUI: C0001145
Disease: Acne Keloid
Acne Keloid 		1 0 1 1.1E-02 0 0
CUI: C0003516
Disease: Aortopulmonary Septal Defect
Aortopulmonary Septal Defect 		1 0 1 1.1E-02 0 0
CUI: C0003708
Disease: Arachnoiditis
Arachnoiditis 		1 0 1 1.1E-02 0 0
CUI: C0007871
Disease: Uterine Cervical Incompetence
Uterine Cervical Incompetence 		1 0 1 1.1E-02 0 0
CUI: C0012767
Disease: Tooth eruption disorder
Tooth eruption disorder 		1 0 1 1.1E-02 0 0
CUI: C0027821
Disease: Neurocirculatory Asthenia
Neurocirculatory Asthenia 		1 0 1 1.1E-02 0 0
CUI: C0029630
Disease: Other heart block
Other heart block 		1 0 1 1.1E-02 0 0
CUI: C0036413
Disease: Scleredema Adultorum
Scleredema Adultorum 		1 0 1 1.1E-02 0 0
CUI: C0038557
Disease: Submandibular Gland Diseases
Submandibular Gland Diseases 		1 0 1 1.1E-02 0 0
CUI: C0151463
Disease: Abscess of breast
Abscess of breast 		1 0 1 1.1E-02 0 0
CUI: C0151482
Disease: Megaloblastic anemia due to folate deficiency
Megaloblastic anemia due to folate deficiency 		1 0 1 1.1E-02 0 0
CUI: C0152091
Disease: Osteochondropathy
Osteochondropathy 		1 0 1 1.1E-02 0 0
CUI: C0155747
Disease: Aneurysm of splenic artery
Aneurysm of splenic artery 		1 0 1 1.1E-02 0 0
CUI: C0157733
Disease: Abnormality of the hair
Abnormality of the hair 		1 0 1 1.1E-02 0 0
CUI: C0158983
Disease: Neonatal thyrotoxicosis
Neonatal thyrotoxicosis 		1 0 1 1.1E-02 0 0
CUI: C0202220
Disease: Somatomedin-C measurement
Somatomedin-C measurement 		1 0 1 1.1E-02 0 0
CUI: C0220743
Disease: Childhood hypophosphatasia (disorder)
Childhood hypophosphatasia (disorder) 		1 0 1 1.1E-02 0 0
CUI: C0231554
Disease: Osteoid formation disorder
Osteoid formation disorder 		1 0 1 1.1E-02 0 0
CUI: C0233643
Disease: Incoherent thinking
Incoherent thinking 		1 0 1 1.1E-02 0 0
CUI: C0235584
Disease: Granulocytopenia severe
Granulocytopenia severe 		1 0 1 1.1E-02 0 0
CUI: C0238185
Disease: Juvenile myxedema
Juvenile myxedema 		1 0 1 1.1E-02 0 0
CUI: C0238590
Disease: Acrogeria
Acrogeria 		1 0 1 1.1E-02 0 0