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: C4476625
Disease: Abnormal temper tantrums
Abnormal temper tantrums 		4 0 2 0.22 0 0
CUI: C0575897
Disease: Thumb deformity
Thumb deformity 		8 7 2 0.15 1 1.0E-01
CUI: C0220982
Disease: Ketoacidosis
Ketoacidosis 		1 0 1 0.14 0 0
CUI: C0235198
Disease: Unable to concentrate
Unable to concentrate 		1 1 1 0.14 1 0.25
CUI: C0279697
Disease: salivary gland squamous cell carcinoma
salivary gland squamous cell carcinoma 		1 0 1 0.14 0 0
CUI: C0334338
Disease: Endometrioid adenoma, borderline malignancy
Endometrioid adenoma, borderline malignancy 		1 0 1 0.14 0 0
CUI: C0334566
Disease: Ghost Cell Odontogenic Carcinoma
Ghost Cell Odontogenic Carcinoma 		1 0 1 0.14 0 0
CUI: C0405124
Disease: Nuchal Cord
Nuchal Cord 		1 1 1 0.14 1 0.25
CUI: C0406571
Disease: Superficial fibromatosis
Superficial fibromatosis 		1 0 1 0.14 0 0
CUI: C0410652
Disease: Cervical spine instability
Cervical spine instability 		1 0 1 0.14 0 0
CUI: C0598675
Disease: inborn aminoaciduria
inborn aminoaciduria 		1 0 1 0.14 0 0
CUI: C0856208
Disease: Increased serum zinc
Increased serum zinc 		1 0 1 0.14 0 0
CUI: C0856823
Disease: Undifferentiated type acute leukemia
Undifferentiated type acute leukemia 		1 0 1 0.14 0 0
CUI: C0862039
Disease: Precursor B-lymphoblastic lymphoma stage II
Precursor B-lymphoblastic lymphoma stage II 		1 0 1 0.14 0 0
CUI: C1275420
Disease: Extra-abdominal fibromatosis
Extra-abdominal fibromatosis 		1 0 1 0.14 0 0
CUI: C1333117
Disease: Colorectal Tubular Adenoma
Colorectal Tubular Adenoma 		1 0 1 0.14 0 0
CUI: C1336727
Disease: Testicular Sarcoma
Testicular Sarcoma 		1 0 1 0.14 0 0
CUI: C1704219
Disease: Dentinogenic Ghost Cell Tumor
Dentinogenic Ghost Cell Tumor 		1 0 1 0.14 0 0
CUI: C1847524
Disease: Hyperopic astigmatism
Hyperopic astigmatism 		9 5 2 0.14 2 0.29
CUI: C3554343
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 17
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17 		1 0 1 0.14 0 0
CUI: C3554449
Disease: MENTAL RETARDATION, AUTOSOMAL DOMINANT 19
MENTAL RETARDATION, AUTOSOMAL DOMINANT 19 		1 21 1 0.14 1 4.2E-02
CUI: C3887926
Disease: CATARACT 32, MULTIPLE TYPES
CATARACT 32, MULTIPLE TYPES 		1 0 1 0.14 0 0
CUI: C4022774
Disease: Focal T2 hyperintense thalamic lesion
Focal T2 hyperintense thalamic lesion 		1 1 1 0.14 1 0.25
CUI: C4022968
Disease: Abnormal hypothalamus physiology
Abnormal hypothalamus physiology 		1 1 1 0.14 1 0.25
CUI: C4023278
Disease: Left aortic arch with retroesophageal right subclavian artery
Left aortic arch with retroesophageal right subclavian artery 		1 1 1 0.14 1 0.25