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: C4551511
Disease: X-linked sideroblastic anemia
X-linked sideroblastic anemia 		16 23 4 8.3E-02 1 4.0E-02
CUI: C1268964
Disease: Myelodysplastic syndrome, no ICD-O subtype
Myelodysplastic syndrome, no ICD-O subtype 		4 0 3 8.1E-02 0 0
CUI: C1292772
Disease: Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative
Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Negative 		32 5 5 7.9E-02 1 0.14
CUI: C0239574
Disease: Low grade fever
Low grade fever 		5 0 3 7.9E-02 0 0
CUI: C0279629
Disease: Adult Acute Monoblastic Leukemia
Adult Acute Monoblastic Leukemia 		19 0 4 7.8E-02 0 0
CUI: C0279645
Disease: Childhood Acute Monoblastic Leukemia
Childhood Acute Monoblastic Leukemia 		19 0 4 7.8E-02 0 0
CUI: C0233397
Disease: Psychological symptom
Psychological symptom 		33 0 5 7.8E-02 0 0
CUI: C1739405
Disease: CML progression
CML progression 		47 0 6 7.8E-02 0 0
CUI: C0023480
Disease: Leukemia, Myelomonocytic, Chronic
Leukemia, Myelomonocytic, Chronic 		158 28 14 7.8E-02 1 3.3E-02
CUI: C0016199
Disease: Flank Pain
Flank Pain 		6 0 3 7.7E-02 0 0
CUI: C0220615
Disease: Adult Acute Myeloblastic Leukemia
Adult Acute Myeloblastic Leukemia 		160 0 14 7.7E-02 0 0
CUI: C0238003
Disease: Adenocarcinoma of appendix
Adenocarcinoma of appendix 		6 0 3 7.7E-02 0 0
CUI: C0272024
Disease: Secondary acquired sideroblastic anemia
Secondary acquired sideroblastic anemia 		6 2 3 7.7E-02 2 0.67
CUI: C1838702
Disease: Retinitis Pigmentosa 13
Retinitis Pigmentosa 13 		6 0 3 7.7E-02 0 0
CUI: C1961835
Disease: Gaucher Disease, Type 1
Gaucher Disease, Type 1 		48 0 6 7.7E-02 0 0
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis 		163 7 14 7.6E-02 1 0.11
CUI: C1512694
Disease: Increased Cellularity Present
Increased Cellularity Present 		21 0 4 7.5E-02 0 0
CUI: C0279549
Disease: Philadelphia chromosome negative chronic myelogenous leukemia
Philadelphia chromosome negative chronic myelogenous leukemia 		7 0 3 7.5E-02 0 0
CUI: C4552670
Disease: Portal Vein Thrombosis, CTCAE
Portal Vein Thrombosis, CTCAE 		7 0 3 7.5E-02 0 0
CUI: C0457334
Disease: Acute monoblastic leukemia
Acute monoblastic leukemia 		37 0 5 7.4E-02 0 0
CUI: C0025167
Disease: Megakaryocytic hyperplasia
Megakaryocytic hyperplasia 		8 1 3 7.3E-02 1 0.33
CUI: C0520477
Disease: Prostatic Adenoma
Prostatic Adenoma 		8 0 3 7.3E-02 0 0
CUI: C1333046
Disease: Myeloproliferative Neoplasm, Unclassifiable
Myeloproliferative Neoplasm, Unclassifiable 		8 3 3 7.3E-02 1 0.20
CUI: C2826177
Disease: Acute myeloid leukemia with mutated NPM1
Acute myeloid leukemia with mutated NPM1 		8 0 3 7.3E-02 0 0
CUI: C0242006
Disease: Myelofibrosis due to another disorder
Myelofibrosis due to another disorder 		23 6 4 7.3E-02 1 0.12