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: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 6 5.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 1 3.2E-03 0 0
CUI: C4022745
Disease: Abnormal basal ganglia MRI signal intensity
Abnormal basal ganglia MRI signal intensity 		7 0 1 6.7E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 0 2 2.2E-03 0 0
CUI: C4025706
Disease: Abnormal globus pallidus morphology
Abnormal globus pallidus morphology 		10 0 1 5.6E-02 0 0
CUI: C1857704
Disease: Abnormal myelination
Abnormal myelination 		49 0 1 1.8E-02 0 0
CUI: C4022448
Disease: Abnormal prolactin level
Abnormal prolactin level 		9 0 1 5.9E-02 0 0
CUI: C4022419
Disease: Abnormal transferrin saturation
Abnormal transferrin saturation 		1 0 1 0.11 0 0
CUI: C1328440
Disease: Abnormality of amino acid metabolism
Abnormality of amino acid metabolism 		8 0 1 6.2E-02 0 0
CUI: C4021768
Disease: Abnormality of metabolism/homeostasis
Abnormality of metabolism/homeostasis 		171 0 2 1.1E-02 0 0
CUI: C4024171
Disease: Abnormality of secondary sexual hair
Abnormality of secondary sexual hair 		7 0 1 6.7E-02 0 0
CUI: C4025819
Disease: Abnormality of the hypothalamus-pituitary axis
Abnormality of the hypothalamus-pituitary axis 		70 0 1 1.3E-02 0 0
CUI: C4021551
Disease: Absence of secondary sex characteristics
Absence of secondary sex characteristics 		44 0 1 1.9E-02 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia 		46 0 2 3.8E-02 0 0
CUI: C0700502
Disease: Acquired hypothyroidism
Acquired hypothyroidism 		13 0 3 0.16 0 0
CUI: C0272362
Disease: Acquired von Willebrand's disease
Acquired von Willebrand's disease 		8 0 1 6.2E-02 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 2 1.4E-02 0 0
CUI: C2718092
Disease: Acrospiroma
Acrospiroma 		12 0 1 5.0E-02 0 0
CUI: C0271583
Disease: ACTH Deficiency, Isolated
ACTH Deficiency, Isolated 		11 0 3 0.18 0 0
CUI: C0234376
Disease: Action Tremor
Action Tremor 		95 0 1 9.7E-03 0 0
CUI: C4023188
Disease: Activating thyroid-stimulating hormone receptor defect
Activating thyroid-stimulating hormone receptor defect 		1 0 1 0.11 0 0
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		1293 0 1 7.7E-04 0 0
CUI: C0023462
Disease: Acute Megakaryocytic Leukemias
Acute Megakaryocytic Leukemias 		159 0 1 6.0E-03 0 0
CUI: C0023487
Disease: Acute Promyelocytic Leukemia
Acute Promyelocytic Leukemia 		651 0 1 1.5E-03 0 0
CUI: C0001403
Disease: Addison Disease
Addison Disease 		111 0 1 8.4E-03 0 0