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: C4049005
Disease: Cataract, total congenital with posterior sutural opacities in Heterozygotes
Cataract, total congenital with posterior sutural opacities in Heterozygotes 		8 0 1 8.3E-02 0 0
CUI: C0349208
Disease: Manic episode
Manic episode 		9 0 1 7.7E-02 0 0
CUI: C4551825
Disease: Megaloblastic Anemia 1
Megaloblastic Anemia 1 		9 0 1 7.7E-02 0 0
CUI: C4025706
Disease: Abnormal globus pallidus morphology
Abnormal globus pallidus morphology 		10 0 1 7.1E-02 0 0
CUI: C3272399
Disease: Gastric Neuroendocrine Tumor
Gastric Neuroendocrine Tumor 		11 0 1 6.7E-02 0 0
CUI: C3812396
Disease: Chronic idiopathic pulmonary fibrosis
Chronic idiopathic pulmonary fibrosis 		11 0 1 6.7E-02 0 0
CUI: C0302845
Disease: MCV - raised
MCV - raised 		12 0 1 6.2E-02 0 0
CUI: C0340782
Disease: Hyperplastic lymph node
Hyperplastic lymph node 		12 0 1 6.2E-02 0 0
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		13 0 2 0.12 0 0
CUI: C0267454
Disease: Necrotic enteritis
Necrotic enteritis 		13 0 1 5.9E-02 0 0
CUI: C0014804
Disease: Erythromelalgia
Erythromelalgia 		14 0 1 5.6E-02 0 0
CUI: C0158458
Disease: Acquired hallux valgus
Acquired hallux valgus 		14 0 1 5.6E-02 0 0
CUI: C0265656
Disease: Congenital hallux valgus
Congenital hallux valgus 		14 0 1 5.6E-02 0 0
CUI: C0268559
Disease: Hyperglycinemia
Hyperglycinemia 		14 0 1 5.6E-02 0 0
CUI: C4523989
Disease: Occult hepatitis B
Occult hepatitis B 		14 0 1 5.6E-02 0 0
CUI: C0002892
Disease: Anemia, Pernicious
Anemia, Pernicious 		16 0 2 0.11 0 0
CUI: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction 		16 0 1 5.0E-02 0 0
CUI: C2004461
Disease: Bowel dysfunction
Bowel dysfunction 		16 0 1 5.0E-02 0 0
CUI: C0268579
Disease: Propionic acidemia
Propionic acidemia 		17 0 1 4.8E-02 0 0
CUI: C0858867
Disease: Reticulocytopenia
Reticulocytopenia 		17 0 1 4.8E-02 0 0
CUI: C0025221
Disease: Meleda Disease
Meleda Disease 		18 0 1 4.5E-02 0 0
CUI: C0206142
Disease: Eosinophilic leukemia
Eosinophilic leukemia 		18 0 1 4.5E-02 0 0
CUI: C0740985
Disease: Acute anaemia
Acute anaemia 		18 0 1 4.5E-02 0 0
CUI: C0848771
Disease: neurological disability
neurological disability 		18 0 1 4.5E-02 0 0
CUI: C1394891
Disease: Intrinsic Factor Deficiency
Intrinsic Factor Deficiency 		18 0 1 4.5E-02 0 0