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: C0334587
Disease: Astroblastoma
Astroblastoma 		6 0 1 0.17 0 0
CUI: C1333989
Disease: Familial meningioma
Familial meningioma 		6 0 1 0.17 0 0
CUI: C4025871
Disease: Abnormality of the face
Abnormality of the face 		31 0 1 3.2E-02 0 0
CUI: C0522631
Disease: Acute myeloid leukemia, minimal differentiation
Acute myeloid leukemia, minimal differentiation 		33 0 1 3.0E-02 0 0
CUI: C0206715
Disease: Neoplasms, Neuroepithelial
Neoplasms, Neuroepithelial 		46 0 1 2.2E-02 0 0
CUI: C0259785
Disease: Malignant Meningioma
Malignant Meningioma 		49 0 1 2.0E-02 0 0
CUI: C1842364
Disease: Central hypotonia
Central hypotonia 		50 0 1 2.0E-02 0 0
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum 		55 0 1 1.8E-02 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology 		70 0 1 1.4E-02 0 0
CUI: C1518922
Disease: peak expiratory flow (procedure)
peak expiratory flow (procedure) 		74 0 1 1.4E-02 0 0
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		80 0 1 1.3E-02 0 0
CUI: C3839868
Disease: Cytogenetically normal acute myeloid leukemia
Cytogenetically normal acute myeloid leukemia 		91 0 1 1.1E-02 0 0
CUI: C0027832
Disease: Neurofibromatosis 2
Neurofibromatosis 2 		127 0 1 7.9E-03 0 0
CUI: C0026998
Disease: Acute Myeloid Leukemia, M1
Acute Myeloid Leukemia, M1 		138 0 1 7.2E-03 0 0
CUI: C0008487
Disease: Chordoma
Chordoma 		140 0 1 7.1E-03 0 0
CUI: C1879321
Disease: Acute Myeloid Leukemia (AML-M2)
Acute Myeloid Leukemia (AML-M2) 		143 0 1 7.0E-03 0 0
CUI: C2981150
Disease: Uranostaphyloschisis
Uranostaphyloschisis 		190 0 1 5.3E-03 0 0
CUI: C0266464
Disease: Polymicrogyria
Polymicrogyria 		199 0 1 5.0E-03 0 0
CUI: C0220621
Disease: Childhood Acute Myeloid Leukemia
Childhood Acute Myeloid Leukemia 		215 0 1 4.7E-03 0 0
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		234 0 1 4.3E-03 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		251 0 1 4.0E-03 0 0
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		265 0 1 3.8E-03 0 0
CUI: C0524587
Disease: Mean Corpuscular Volume (result)
Mean Corpuscular Volume (result) 		269 0 1 3.7E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 3.7E-03 0 0
CUI: C1837218
Disease: Cleft palate, isolated
Cleft palate, isolated 		295 0 1 3.4E-03 0 0