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: C0154307
Disease: Banti's syndrome
Banti's syndrome 		8 0 3 0.21 0 0
CUI: C0546953
Disease: Subacromial bursitis
Subacromial bursitis 		8 0 3 0.21 0 0
CUI: C0524988
Disease: Schnitzler Syndrome
Schnitzler Syndrome 		14 0 4 0.21 0 0
CUI: C0014077
Disease: Leukoencephalitis, Acute Hemorrhagic
Leukoencephalitis, Acute Hemorrhagic 		9 0 3 0.20 0 0
CUI: C0151828
Disease: Injection site pain
Injection site pain 		3 0 2 0.20 0 0
CUI: C0242993
Disease: Nephropathia Epidemica
Nephropathia Epidemica 		9 0 3 0.20 0 0
CUI: C0263949
Disease: Proliferative synovitis
Proliferative synovitis 		3 0 2 0.20 0 0
CUI: C0268405
Disease: Hemodialysis-associated amyloidosis
Hemodialysis-associated amyloidosis 		3 0 2 0.20 0 0
CUI: C0281774
Disease: Acute psychosis
Acute psychosis 		3 0 2 0.20 0 0
CUI: C0282312
Disease: Bubonic Plague
Bubonic Plague 		3 0 2 0.20 0 0
CUI: C0406735
Disease: Hypoplastic enamel-onycholysis-hypohidrosis syndrome
Hypoplastic enamel-onycholysis-hypohidrosis syndrome 		3 0 2 0.20 0 0
CUI: C0863129
Disease: AGEP
AGEP 		9 0 3 0.20 0 0
CUI: C1849678
Disease: Peroxisomal ACYL-COA oxidase deficiency
Peroxisomal ACYL-COA oxidase deficiency 		3 0 2 0.20 0 0
CUI: C1876187
Disease: TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL 		9 0 3 0.20 0 0
CUI: C1971635
Disease: Scleritis and episcleritis (disorder)
Scleritis and episcleritis (disorder) 		3 0 2 0.20 0 0
CUI: C2748507
Disease: INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY
INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCY 		3 0 2 0.20 0 0
CUI: C2939127
Disease: Indolent ulcer
Indolent ulcer 		3 0 2 0.20 0 0
CUI: C3829514
Disease: Intrapartum fever
Intrapartum fever 		3 0 2 0.20 0 0
CUI: C3839524
Disease: Anemia in malignant neoplastic disease
Anemia in malignant neoplastic disease 		3 0 2 0.20 0 0
CUI: C4707790
Disease: Idiopathic recurrent pericarditis
Idiopathic recurrent pericarditis 		3 0 2 0.20 0 0
CUI: C4722480
Disease: PLCG2-associated antibody deficiency and immune dysregulation
PLCG2-associated antibody deficiency and immune dysregulation 		3 0 2 0.20 0 0
CUI: C0024959
Disease: Maxillary Sinusitis
Maxillary Sinusitis 		10 0 3 0.19 0 0
CUI: C0795996
Disease: STRIATONIGRAL DEGENERATION, INFANTILE (disorder)
STRIATONIGRAL DEGENERATION, INFANTILE (disorder) 		10 0 3 0.19 0 0
CUI: C1455718
Disease: Neurological ventriculitis
Neurological ventriculitis 		10 0 3 0.19 0 0
CUI: C3160844
Disease: PAI-1 polymorphism
PAI-1 polymorphism 		10 0 3 0.19 0 0