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: C2675526
Disease: Neutropenia, Severe Congenital, Autosomal Recessive 4
Neutropenia, Severe Congenital, Autosomal Recessive 4 		1 0 1 1.00 0 0
CUI: C2751630
Disease: Dursun Syndrome
Dursun Syndrome 		1 0 1 1.00 0 0
CUI: C0427543
Disease: Increased blood monocyte number
Increased blood monocyte number 		8 0 1 0.12 0 0
CUI: C0268146
Disease: Glucose-6-phosphate transport defect
Glucose-6-phosphate transport defect 		9 0 1 0.11 0 0
CUI: C2919796
Disease: Glycogen storage disease type Ia
Glycogen storage disease type Ia 		10 0 1 1.0E-01 0 0
CUI: C0272173
Disease: Myelokathexis
Myelokathexis 		11 0 1 9.1E-02 0 0
CUI: C0542035
Disease: Erythroid hypoplasia
Erythroid hypoplasia 		14 0 1 7.1E-02 0 0
CUI: C0272183
Disease: Qualitative abnormality of granulocyte
Qualitative abnormality of granulocyte 		22 0 1 4.5E-02 0 0
CUI: C0017920
Disease: Glycogen Storage Disease Type I
Glycogen Storage Disease Type I 		24 0 1 4.2E-02 0 0
CUI: C3890737
Disease: Autoinflammatory Syndrome
Autoinflammatory Syndrome 		25 0 1 4.0E-02 0 0
CUI: C3495549
Disease: Patent ductus arteriosus - persisting type
Patent ductus arteriosus - persisting type 		30 0 1 3.3E-02 0 0
CUI: C0685891
Disease: Congenital hypoplasia of thymus
Congenital hypoplasia of thymus 		34 0 1 2.9E-02 0 0
CUI: C0344724
Disease: Ostium secundum atrial septal defect
Ostium secundum atrial septal defect 		37 0 1 2.7E-02 0 0
CUI: C0042063
Disease: Urogenital Abnormalities
Urogenital Abnormalities 		42 0 1 2.4E-02 0 0
CUI: C0078918
Disease: Albinism, Oculocutaneous
Albinism, Oculocutaneous 		49 0 1 2.0E-02 0 0
CUI: C0151721
Disease: Testicular hypogonadism
Testicular hypogonadism 		50 0 1 2.0E-02 0 0
CUI: C0221023
Disease: Cyclic neutropenia
Cyclic neutropenia 		52 0 1 1.9E-02 0 0
CUI: C0085702
Disease: Monocytosis
Monocytosis 		61 0 1 1.6E-02 0 0
CUI: C0017919
Disease: Glycogen Storage Disease
Glycogen Storage Disease 		63 0 1 1.6E-02 0 0
CUI: C1853118
Disease: Severe congenital neutropenia
Severe congenital neutropenia 		66 0 1 1.5E-02 0 0
CUI: C0426891
Disease: Broad thumbs
Broad thumbs 		67 0 1 1.5E-02 0 0
CUI: C0340970
Disease: Congenital neutropenia
Congenital neutropenia 		68 0 1 1.5E-02 0 0
CUI: C1844383
Disease: Recurrent bacterial infection
Recurrent bacterial infection 		69 0 1 1.4E-02 0 0
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent 		73 0 1 1.4E-02 0 0
CUI: C0424731
Disease: Single transverse palmar crease
Single transverse palmar crease 		78 0 1 1.3E-02 0 0