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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 0.33
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 2 0.33
CUI: C0342788
Disease: Renal carnitine transport defect
Renal carnitine transport defect 		0 123 0 0 1 8.0E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 0.33
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 0.33
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 0.25
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 0.20
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		291 0 1 2.2E-03 0 0
CUI: C0202239
Disease: Uric acid measurement (procedure)
Uric acid measurement (procedure) 		264 0 1 2.3E-03 0 0
CUI: C0153594
Disease: Malignant neoplasm of testis
Malignant neoplasm of testis 		253 0 1 2.4E-03 0 0
CUI: C0489786
Disease: Height
Height 		249 0 1 2.4E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 2.5E-03 0 0
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex 		218 0 1 2.6E-03 0 0
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia 		216 0 1 2.6E-03 0 0
CUI: C0333068
Disease: Flexion contracture
Flexion contracture 		210 0 1 2.6E-03 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		198 0 1 2.7E-03 0 0
CUI: C1845847
Disease: Coarse facial features
Coarse facial features 		194 0 1 2.7E-03 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders 		183 0 1 2.8E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		176 0 1 2.9E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia 		172 0 1 2.9E-03 0 0
CUI: C1845977
Disease: X- linked recessive
X- linked recessive 		172 0 1 2.9E-03 0 0
CUI: C0596887
Disease: mathematical ability
mathematical ability 		854 0 3 2.9E-03 0 0
CUI: C0024003
Disease: Lordosis
Lordosis 		160 0 1 3.0E-03 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead 		159 0 1 3.0E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		158 0 1 3.0E-03 0 0