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: C0375206
Disease: Hemiplegia/hemiparesis
Hemiplegia/hemiparesis 		112 2 4 9.9E-03 1 0.14
CUI: C0494475
Disease: Tonic - clonic seizures
Tonic - clonic seizures 		300 32 25 4.4E-02 1 2.7E-02
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		480 105 58 8.1E-02 1 9.1E-03
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		1825 553 77 3.8E-02 1 1.8E-03
CUI: C0699790
Disease: Colon Carcinoma
Colon Carcinoma 		2832 275 122 4.1E-02 1 3.6E-03
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		321 67 12 2.0E-02 1 1.4E-02
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		8221 1374 226 2.7E-02 1 7.3E-04
CUI: C1837142
Disease: Poor suck
Poor suck 		103 31 4 1.0E-02 1 2.8E-02
CUI: C1838993
Disease: Episodic vomiting
Episodic vomiting 		43 10 2 6.0E-03 1 6.7E-02
CUI: C1840437
Disease: Isolated hyperchlorhidrosis
Isolated hyperchlorhidrosis 		1 5 1 3.4E-03 1 1.0E-01
CUI: C1857287
Disease: Stroke-like episode
Stroke-like episode 		27 3 1 3.1E-03 1 0.12
CUI: C1859236
Disease: Prolonged neonatal jaundice
Prolonged neonatal jaundice 		59 14 2 5.7E-03 1 5.3E-02
CUI: C2237142
Disease: Moderate global developmental delay
Moderate global developmental delay 		27 21 3 9.4E-03 1 3.8E-02
CUI: C3887485
Disease: MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1 		20 19 2 6.4E-03 1 4.2E-02
CUI: C4225242
Disease: DEHYDRATED HEREDITARY STOMATOCYTOSIS 2
DEHYDRATED HEREDITARY STOMATOCYTOSIS 2 		1 3 1 3.4E-03 1 0.12
CUI: C4316903
Disease: Absence Seizures
Absence Seizures 		205 8 13 2.7E-02 1 7.7E-02
CUI: C4551520
Disease: Intention tremor
Intention tremor 		20 6 1 3.2E-03 1 9.1E-02
CUI: C0000731
Disease: Abdomen distended
Abdomen distended 		103 0 7 1.8E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain 		302 0 26 4.6E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia 		65 0 8 2.3E-02 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality 		1098 0 62 4.7E-02 0 0
CUI: C0000771
Disease: Abnormalities, Drug-Induced
Abnormalities, Drug-Induced 		5 0 1 3.3E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 12 2.2E-02 0 0
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion 		188 0 9 1.9E-02 0 0
CUI: C0000809
Disease: Abortion, Habitual
Abortion, Habitual 		7 0 1 3.3E-03 0 0