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: C0279582
Disease: Childhood Burkitt Leukemia
Childhood Burkitt Leukemia 		10 0 2 0.11 0 0
CUI: C0279591
Disease: Adult Burkitt Leukemia
Adult Burkitt Leukemia 		10 0 2 0.11 0 0
CUI: C4288893
Disease: Infant Acute Biphenotypic Leukemia
Infant Acute Biphenotypic Leukemia 		10 0 2 0.11 0 0
CUI: C1327920
Disease: Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive
Childhood Chronic Myelogenous Leukemia, BCR-ABL1 Positive 		12 0 2 9.5E-02 0 0
CUI: C0007939
Disease: Syphilitic chancre
Syphilitic chancre 		1 0 1 9.1E-02 0 0
CUI: C0231246
Disease: Failure to gain weight
Failure to gain weight 		1 2 1 9.1E-02 1 0.20
CUI: C0410652
Disease: Cervical spine instability
Cervical spine instability 		1 0 1 9.1E-02 0 0
CUI: C0431501
Disease: Bilateral arterial duct
Bilateral arterial duct 		1 0 1 9.1E-02 0 0
CUI: C0751575
Disease: Paralysis, Unilateral, Vocal Cord
Paralysis, Unilateral, Vocal Cord 		1 0 1 9.1E-02 0 0
CUI: C0856823
Disease: Undifferentiated type acute leukemia
Undifferentiated type acute leukemia 		1 0 1 9.1E-02 0 0
CUI: C0862039
Disease: Precursor B-lymphoblastic lymphoma stage II
Precursor B-lymphoblastic lymphoma stage II 		1 0 1 9.1E-02 0 0
CUI: C1336727
Disease: Testicular Sarcoma
Testicular Sarcoma 		1 0 1 9.1E-02 0 0
CUI: C1832812
Disease: Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation
Cataracts, Congenital, with Sensorineural Deafness, Down Syndrome-Like Facial Appearance, Short Stature, and Mental Retardation 		1 0 1 9.1E-02 0 0
CUI: C1857768
Disease: Cataract, Pulverulent, Juvenile-Onset
Cataract, Pulverulent, Juvenile-Onset 		1 0 1 9.1E-02 0 0
CUI: C2676770
Disease: Birk-Barel Mental Retardation Dysmorphism Syndrome
Birk-Barel Mental Retardation Dysmorphism Syndrome 		1 0 1 9.1E-02 0 0
CUI: C2931317
Disease: Primary syphilis
Primary syphilis 		1 0 1 9.1E-02 0 0
CUI: C3280127
Disease: MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 		1 0 1 9.1E-02 0 0
CUI: C3888097
Disease: CATARACT 21, MULTIPLE TYPES
CATARACT 21, MULTIPLE TYPES 		1 0 1 9.1E-02 0 0
CUI: C4016396
Disease: LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB
LEUKEMIA, PHILADELPHIA CHROMOSOME-POSITIVE, RESISTANT TO IMATINIB 		1 0 1 9.1E-02 0 0
CUI: C4021943
Disease: Abnormality of the xiphoid process
Abnormality of the xiphoid process 		1 0 1 9.1E-02 0 0
CUI: C4023165
Disease: Abnormality of skeletal morphology
Abnormality of skeletal morphology 		1 2 1 9.1E-02 1 0.20
CUI: C4023544
Disease: Incisor macrodontia
Incisor macrodontia 		1 0 1 9.1E-02 0 0
CUI: C4023625
Disease: Absence of stomach bubble on fetal sonography
Absence of stomach bubble on fetal sonography 		1 1 1 9.1E-02 1 0.25
CUI: C4023694
Disease: Abnormal position of hair whorl
Abnormal position of hair whorl 		1 0 1 9.1E-02 0 0
CUI: C4024836
Disease: Generalized reticulate brown pigmentation
Generalized reticulate brown pigmentation 		1 0 1 9.1E-02 0 0