Source: CURATED ×
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: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		173 6669 7 1.6E-02 3 4.4E-04
CUI: C0027672
Disease: Neoplastic Syndromes, Hereditary
Neoplastic Syndromes, Hereditary 		0 6385 0 0 1 1.5E-04
CUI: C2675520
Disease: BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2
BREAST-OVARIAN CANCER, FAMILIAL, SUSCEPTIBILITY TO, 2 		0 2633 0 0 1 3.6E-04
CUI: C0677776
Disease: Hereditary Breast and Ovarian Cancer Syndrome
Hereditary Breast and Ovarian Cancer Syndrome 		14 2106 1 3.6E-03 1 4.4E-04
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		221 1232 9 1.9E-02 1 7.1E-04
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0 1138 0 0 1 7.6E-04
CUI: C0024796
Disease: Marfan Syndrome
Marfan Syndrome 		11 997 2 7.4E-03 1 8.5E-04
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0 988 0 0 1 8.6E-04
CUI: C1304746
Disease: RDW - Red blood cell distribution width result
RDW - Red blood cell distribution width result 		0 988 0 0 1 8.6E-04
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0 611 0 0 3 3.8E-03
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia 		17 579 2 7.2E-03 10 1.3E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		477 552 65 9.7E-02 1 1.4E-03
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		133 505 14 3.7E-02 20 3.0E-02
CUI: C0027404
Disease: Narcolepsy
Narcolepsy 		17 447 1 3.6E-03 1 1.6E-03
CUI: C4707243
Disease: Familial thoracic aortic aneurysm and aortic dissection
Familial thoracic aortic aneurysm and aortic dissection 		0 442 0 0 1 1.6E-03
CUI: C0036572
Disease: Seizures
Seizures 		218 417 28 6.2E-02 22 3.8E-02
CUI: C1843367
Disease: Poor school performance
Poor school performance 		0 411 0 0 15 2.6E-02
CUI: C4551549
Disease: Early Infantile Epileptic Encephalopathy 6
Early Infantile Epileptic Encephalopathy 6 		0 392 0 0 1 1.7E-03
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		3 379 1 3.8E-03 1 1.8E-03
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		17 350 2 7.2E-03 1 1.9E-03
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		5 339 3 1.1E-02 3 5.8E-03
CUI: C0349588
Disease: Short stature
Short stature 		0 292 0 0 3 6.4E-03
CUI: C1384666
Disease: hearing impairment
hearing impairment 		98 261 2 5.6E-03 2 4.5E-03
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		0 246 0 0 8 1.9E-02
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism 		4 245 1 3.8E-03 1 2.4E-03