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: C4290088
Disease: decreased absolute neurophile count (ANC)
decreased absolute neurophile count (ANC) 		1 0 1 1.00 0 0
CUI: C0272167
Disease: Reticular dysgenesis
Reticular dysgenesis 		2 0 1 0.50 0 0
CUI: C1842930
Disease: Neutropenia, Nonimmune Chronic Idiopathic, Adult
Neutropenia, Nonimmune Chronic Idiopathic, Adult 		2 0 1 0.50 0 0
CUI: C1859966
Disease: Neutropenia, Severe Congenital, Autosomal Dominant 1
Neutropenia, Severe Congenital, Autosomal Dominant 1 		4 0 1 0.25 0 0
CUI: C2931027
Disease: Neutropenia, severe chronic
Neutropenia, severe chronic 		6 0 1 0.17 0 0
CUI: C0427543
Disease: Increased blood monocyte number
Increased blood monocyte number 		8 0 1 0.12 0 0
CUI: C2267231
Disease: Chronic idiopathic neutropenia
Chronic idiopathic neutropenia 		10 0 1 1.0E-01 0 0
CUI: C0398593
Disease: Specific granule deficiency
Specific granule deficiency 		11 0 1 9.1E-02 0 0
CUI: C0743360
Disease: Recurrent ear infections
Recurrent ear infections 		11 0 1 9.1E-02 0 0
CUI: C1855067
Disease: B lymphocytopenia
B lymphocytopenia 		13 0 1 7.7E-02 0 0
CUI: C1858981
Disease: Antineutrophil antibody positivity
Antineutrophil antibody positivity 		15 0 1 6.7E-02 0 0
CUI: C1846546
Disease: Recurrent sinopulmonary infections
Recurrent sinopulmonary infections 		16 0 1 6.2E-02 0 0
CUI: C1854495
Disease: Recurrent infection of the gastrointestinal tract
Recurrent infection of the gastrointestinal tract 		16 0 1 6.2E-02 0 0
CUI: C0232513
Disease: Premature tooth loss
Premature tooth loss 		25 0 1 4.0E-02 0 0
CUI: C1706004
Disease: Anhydrotic Ectodermal Dysplasias
Anhydrotic Ectodermal Dysplasias 		29 0 1 3.4E-02 0 0
CUI: C0031350
Disease: Pharyngitis
Pharyngitis 		30 0 1 3.3E-02 0 0
CUI: C1837066
Disease: Recurrent viral infection
Recurrent viral infection 		32 0 1 3.1E-02 0 0
CUI: C0752122
Disease: Spinocerebellar Ataxia Type 4
Spinocerebellar Ataxia Type 4 		36 0 1 2.8E-02 0 0
CUI: C0007642
Disease: Cellulitis
Cellulitis 		38 0 1 2.6E-02 0 0
CUI: C2930967
Disease: Gastro-enteropancreatic neuroendocrine tumor
Gastro-enteropancreatic neuroendocrine tumor 		41 0 1 2.4E-02 0 0
CUI: C0001768
Disease: Agammaglobulinemia
Agammaglobulinemia 		43 0 1 2.3E-02 0 0
CUI: C0162359
Disease: Christ-Siemens-Touraine syndrome
Christ-Siemens-Touraine syndrome 		45 0 1 2.2E-02 0 0
CUI: C0085652
Disease: Pyoderma Gangrenosum
Pyoderma Gangrenosum 		47 0 1 2.1E-02 0 0
CUI: C0752123
Disease: Spinocerebellar Ataxia Type 5
Spinocerebellar Ataxia Type 5 		48 0 1 2.1E-02 0 0
CUI: C1332153
Disease: acute myeloid leukemia with multilineage dysplasia following myelodysplastic syndrome
acute myeloid leukemia with multilineage dysplasia following myelodysplastic syndrome 		49 0 1 2.0E-02 0 0