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: C0206717
Disease: Olfactory Neuroblastoma
Olfactory Neuroblastoma 		38 0 7 6.2E-02 0 0
CUI: C0238284
Disease: Acute mountain sickness
Acute mountain sickness 		21 0 6 6.2E-02 0 0
CUI: C0432474
Disease: Klinefelter's syndrome - male with more than two X chromosomes
Klinefelter's syndrome - male with more than two X chromosomes 		90 5 10 6.2E-02 1 3.8E-02
CUI: C0085413
Disease: Polycystic Kidney, Autosomal Dominant
Polycystic Kidney, Autosomal Dominant 		280 0 21 6.2E-02 0 0
CUI: C0014800
Disease: Erythroid hyperplasia
Erythroid hyperplasia 		22 3 6 6.1E-02 1 4.2E-02
CUI: C0233746
Disease: Perceptual disturbance
Perceptual disturbance 		5 0 5 6.1E-02 0 0
CUI: C0240066
Disease: Iron deficiency
Iron deficiency 		179 13 15 6.1E-02 1 2.9E-02
CUI: C0242006
Disease: Myelofibrosis due to another disorder
Myelofibrosis due to another disorder 		23 6 6 6.1E-02 1 3.7E-02
CUI: C1708353
Disease: Hereditary Paraganglioma-Pheochromocytoma Syndrome
Hereditary Paraganglioma-Pheochromocytoma Syndrome 		23 0 6 6.1E-02 0 0
CUI: C0021151
Disease: Incipient Schizophrenia
Incipient Schizophrenia 		6 0 5 6.0E-02 0 0
CUI: C2347748
Disease: Adult Erythroleukemia
Adult Erythroleukemia 		236 4 18 6.0E-02 1 4.0E-02
CUI: C4520840
Disease: Erythroleukemia (Erythroid/Myeloid)
Erythroleukemia (Erythroid/Myeloid) 		237 4 18 6.0E-02 1 4.0E-02
CUI: C0239935
Disease: Hematocrit increased
Hematocrit increased 		7 0 5 6.0E-02 0 0
CUI: C0549448
Disease: Hemoglobin increased
Hemoglobin increased 		7 0 5 6.0E-02 0 0
CUI: C0730315
Disease: Acute central serous chorioretinopathy
Acute central serous chorioretinopathy 		7 0 5 6.0E-02 0 0
CUI: C0240805
Disease: Prodrome
Prodrome 		10 0 5 5.7E-02 0 0
CUI: C1846006
Disease: Ectodermal dysplasia, hypohidrotic, with immune deficiency
Ectodermal dysplasia, hypohidrotic, with immune deficiency 		10 0 5 5.7E-02 0 0
CUI: C1565662
Disease: Acute Kidney Insufficiency
Acute Kidney Insufficiency 		104 0 10 5.7E-02 0 0
CUI: C0410207
Disease: Tubular Aggregate Myopathy
Tubular Aggregate Myopathy 		67 0 8 5.7E-02 0 0
CUI: C1834582
Disease: MYELOPROLIFERATIVE SYNDROME, TRANSIENT
MYELOPROLIFERATIVE SYNDROME, TRANSIENT 		105 0 10 5.6E-02 0 0
CUI: C0018671
Disease: Head and Neck Neoplasms
Head and Neck Neoplasms 		124 0 11 5.6E-02 0 0
CUI: C0025637
Disease: Methemoglobinemia
Methemoglobinemia 		12 0 5 5.6E-02 0 0
CUI: C0026987
Disease: Myelofibrosis
Myelofibrosis 		163 7 13 5.6E-02 1 3.6E-02
CUI: C0030421
Disease: Paraganglioma
Paraganglioma 		165 0 13 5.6E-02 0 0
CUI: C0178540
Disease: Cerebral Hypoxia-Ischemia
Cerebral Hypoxia-Ischemia 		13 0 5 5.6E-02 0 0