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: C2047886
Disease: (Idiopathic) normal pressure hydrocephalus
(Idiopathic) normal pressure hydrocephalus 		14 0 1 2.5E-02 0 0
CUI: C2936346
Disease: 22q11 Deletion Syndrome
22q11 Deletion Syndrome 		31 0 1 1.8E-02 0 0
CUI: C1142214
Disease: Abdominal cocoon
Abdominal cocoon 		1 0 1 3.7E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		910 0 9 9.7E-03 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination 		59 0 1 1.2E-02 0 0
CUI: C0392702
Disease: Abnormal involuntary movement
Abnormal involuntary movement 		22 0 1 2.1E-02 0 0
CUI: C0392188
Disease: Abnormal rapid eye movement sleep
Abnormal rapid eye movement sleep 		11 0 1 2.7E-02 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision 		127 0 1 6.5E-03 0 0
CUI: C1855852
Disease: Abnormally large globe
Abnormally large globe 		16 0 1 2.4E-02 0 0
CUI: C0000833
Disease: Abscess
Abscess 		96 0 1 8.2E-03 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy 		89 0 2 1.8E-02 0 0
CUI: C0278134
Disease: Absence of sensation
Absence of sensation 		111 0 1 7.3E-03 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 0 3 1.3E-02 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 3.9E-03 0 0
CUI: C2936664
Disease: Acquired Hypogammaglobulinemia
Acquired Hypogammaglobulinemia 		89 0 1 8.7E-03 0 0
CUI: C0700502
Disease: Acquired hypothyroidism
Acquired hypothyroidism 		13 0 1 2.6E-02 0 0
CUI: C0001175
Disease: Acquired Immunodeficiency Syndrome
Acquired Immunodeficiency Syndrome 		243 0 1 3.7E-03 0 0
CUI: C1836232
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		147 0 1 5.8E-03 0 0
CUI: C0751919
Disease: Acquired Neuromyotonia
Acquired Neuromyotonia 		4 0 2 6.9E-02 0 0
CUI: C0272362
Disease: Acquired von Willebrand's disease
Acquired von Willebrand's disease 		8 0 1 2.9E-02 0 0
CUI: C0220659
Disease: Acrodysostosis
Acrodysostosis 		31 0 1 1.8E-02 0 0
CUI: C0001206
Disease: Acromegaly
Acromegaly 		138 0 1 6.1E-03 0 0
CUI: C0271583
Disease: ACTH Deficiency, Isolated
ACTH Deficiency, Isolated 		11 0 1 2.7E-02 0 0
CUI: C0001231
Disease: ACTH Syndrome, Ectopic
ACTH Syndrome, Ectopic 		11 0 1 2.7E-02 0 0
CUI: C1857451
Disease: Acth-Independent Macronodular Adrenal Hyperplasia
Acth-Independent Macronodular Adrenal Hyperplasia 		46 0 1 1.4E-02 0 0