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: C4025612
Disease: Polyclonal elevation of IgM
Polyclonal elevation of IgM 		5 0 2 0.29 0 0
CUI: C0026471
Disease: Monoclonal paraproteinemia
Monoclonal paraproteinemia 		1 0 1 0.25 0 0
CUI: C0332885
Disease: Congenital stenosis
Congenital stenosis 		1 0 1 0.25 0 0
CUI: C0877313
Disease: Neonatal neuroblastoma
Neonatal neuroblastoma 		1 0 1 0.25 0 0
CUI: C1262216
Disease: IgM gammopathy
IgM gammopathy 		1 0 1 0.25 0 0
CUI: C1707549
Disease: Cutaneous Lymphomatoid Granulomatosis
Cutaneous Lymphomatoid Granulomatosis 		1 0 1 0.25 0 0
CUI: C1833275
Disease: Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative
Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, NK Cell-Negative 		1 0 1 0.25 0 0
CUI: C1834821
Disease: METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS
METAPHYSEAL DYSPLASIA WITHOUT HYPOTRICHOSIS 		1 0 1 0.25 0 0
CUI: C1835192
Disease: MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1
MACROGLOBULINEMIA, WALDENSTROM, SUSCEPTIBILITY TO, 1 		1 0 1 0.25 0 0
CUI: C1855205
Disease: Susceptibility to chickenpox
Susceptibility to chickenpox 		1 0 1 0.25 0 0
CUI: C2017869
Disease: sparse facial hair
sparse facial hair 		1 0 1 0.25 0 0
CUI: C2350879
Disease: Tropical Eosinophilic Pneumonia
Tropical Eosinophilic Pneumonia 		1 0 1 0.25 0 0
CUI: C2936755
Disease: Familial Waldenstrom's Macroglobulinaemia
Familial Waldenstrom's Macroglobulinaemia 		1 0 1 0.25 0 0
CUI: C4023167
Disease: Partial IgA deficiency
Partial IgA deficiency 		1 0 1 0.25 0 0
CUI: C4073163
Disease: Absent natural killer cells
Absent natural killer cells 		1 0 1 0.25 0 0
CUI: C4477091
Disease: Monoclonal immunoglobulin M proteinemia
Monoclonal immunoglobulin M proteinemia 		1 0 1 0.25 0 0
CUI: C4551965
Disease: ANAUXETIC DYSPLASIA 1
ANAUXETIC DYSPLASIA 1 		1 0 1 0.25 0 0
CUI: C0153504
Disease: Malignant tumor of mediastinum
Malignant tumor of mediastinum 		2 0 1 0.20 0 0
CUI: C0221030
Disease: Hyperviscosity syndrome
Hyperviscosity syndrome 		2 0 1 0.20 0 0
CUI: C0259743
Disease: Autosomal recessive SCID
Autosomal recessive SCID 		2 0 1 0.20 0 0
CUI: C0451694
Disease: Severe combined immunodeficiency with low or normal B-cell numbers
Severe combined immunodeficiency with low or normal B-cell numbers 		2 0 1 0.20 0 0
CUI: C1846796
Disease: Anauxetic dysplasia
Anauxetic dysplasia 		2 0 1 0.20 0 0
CUI: C1855196
Disease: Flaring of lower rib cage
Flaring of lower rib cage 		2 0 1 0.20 0 0
CUI: C4476965
Disease: Absent pubertal growth spurt
Absent pubertal growth spurt 		2 0 1 0.20 0 0
CUI: C4479357
Disease: ANAUXETIC DYSPLASIA 2
ANAUXETIC DYSPLASIA 2 		2 0 1 0.20 0 0