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: C4225221
Disease: RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2
RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 2 		1 0 1 0.33 0 0
CUI: C4551975
Disease: RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 1
RADIOULNAR SYNOSTOSIS WITH AMEGAKARYOCYTIC THROMBOCYTOPENIA 1 		1 0 1 0.33 0 0
CUI: C4744720
Disease: High Risk Acute Myeloid Leukemia
High Risk Acute Myeloid Leukemia 		6 0 2 0.29 0 0
CUI: C0398639
Disease: Amegakaryocytic thrombocytopenia
Amegakaryocytic thrombocytopenia 		7 0 2 0.25 0 0
CUI: C0740268
Disease: Pelvic prolapse
Pelvic prolapse 		2 0 1 0.25 0 0
CUI: C1292775
Disease: Acute myeloid leukemia, 11q23 abnormalities
Acute myeloid leukemia, 11q23 abnormalities 		7 0 2 0.25 0 0
CUI: C1327915
Disease: Congenital amegakaryocytic thrombocytopenia
Congenital amegakaryocytic thrombocytopenia 		7 0 2 0.25 0 0
CUI: C1861331
Disease: Limited pronation/supination of forearm
Limited pronation/supination of forearm 		7 0 2 0.25 0 0
CUI: C0334674
Disease: Acute panmyelosis with myelofibrosis
Acute panmyelosis with myelofibrosis 		8 0 2 0.22 0 0
CUI: C0267532
Disease: Diversion colitis
Diversion colitis 		3 0 1 0.20 0 0
CUI: C1320638
Disease: Bone marrow myeloid dysplasia
Bone marrow myeloid dysplasia 		9 0 2 0.20 0 0
CUI: C1858312
Disease: Megakaryocytopenia
Megakaryocytopenia 		3 0 1 0.20 0 0
CUI: C3280030
Disease: GATA2 Deficiency
GATA2 Deficiency 		9 0 2 0.20 0 0
CUI: C0280028
Disease: Refractory anemia with excess blasts in transformation (clinical)
Refractory anemia with excess blasts in transformation (clinical) 		10 0 2 0.18 0 0
CUI: C0280745
Disease: secondary myelodysplastic syndromes
secondary myelodysplastic syndromes 		11 0 2 0.17 0 0
CUI: C0272278
Disease: Congenital thrombocytopenia
Congenital thrombocytopenia 		19 0 3 0.16 0 0
CUI: C1275661
Disease: Acute myeloid leukemia with recurrent genetic abnormality
Acute myeloid leukemia with recurrent genetic abnormality 		5 0 1 0.14 0 0
CUI: C2676443
Disease: Proximal radio-ulnar synostosis
Proximal radio-ulnar synostosis 		5 0 1 0.14 0 0
CUI: C0152240
Disease: Uterus bilocularis
Uterus bilocularis 		6 0 1 0.12 0 0
CUI: C0373675
Disease: Magnesium measurement
Magnesium measurement 		7 0 1 0.11 0 0
CUI: C0745581
Disease: knee symptoms
knee symptoms 		7 0 1 0.11 0 0
CUI: C1854910
Disease: Shallow acetabular fossae
Shallow acetabular fossae 		8 0 1 1.0E-01 0 0
CUI: C2986691
Disease: Inherited bone marrow failure syndrome
Inherited bone marrow failure syndrome 		11 0 1 7.7E-02 0 0
CUI: C0175703
Disease: Thrombocytopenia-Absent Radius Syndrome
Thrombocytopenia-Absent Radius Syndrome 		12 0 1 7.1E-02 0 0
CUI: C1865847
Disease: Ulnar bowing
Ulnar bowing 		12 0 1 7.1E-02 0 0