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: C0268417
Disease: Pancreatic trypsinogen deficiency
Pancreatic trypsinogen deficiency 		0 1 0 0 1 2.6E-02
CUI: C0334419
Disease: Pheochromocytoma, malignant
Pheochromocytoma, malignant 		0 1 0 0 1 2.6E-02
CUI: C1855801
Disease: Calcium nephrolithiasis
Calcium nephrolithiasis 		0 1 0 0 1 2.6E-02
CUI: C4025337
Disease: Abnormality of calcium homeostasis
Abnormality of calcium homeostasis 		0 1 0 0 1 2.6E-02
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		717 0 1 1.2E-03 0 0
CUI: C1261502
Disease: Finding of Mean Corpuscular Hemoglobin
Finding of Mean Corpuscular Hemoglobin 		653 0 1 1.3E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 1 1.3E-03 0 0
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		578 0 1 1.4E-03 0 0
CUI: C4553743
Disease: Spasticity, CTCAE
Spasticity, CTCAE 		477 0 1 1.7E-03 0 0
CUI: C0013421
Disease: Dystonia
Dystonia 		453 0 1 1.8E-03 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		441 0 1 1.8E-03 0 0
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		429 0 1 1.8E-03 0 0
CUI: C3278923
Disease: Dilated ventricles (finding)
Dilated ventricles (finding) 		427 0 1 1.8E-03 0 0
CUI: C1531647
Disease: Cerebral ventriculomegaly
Cerebral ventriculomegaly 		410 0 1 1.9E-03 0 0
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		401 0 1 1.9E-03 0 0
CUI: C1836830
Disease: Developmental regression
Developmental regression 		333 0 1 2.2E-03 0 0
CUI: C0151888
Disease: Hyporeflexia
Hyporeflexia 		312 0 1 2.3E-03 0 0
CUI: C0521525
Disease: Short neck
Short neck 		288 0 1 2.5E-03 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		285 0 1 2.5E-03 0 0
CUI: C0016202
Disease: Flatfoot
Flatfoot 		285 0 1 2.5E-03 0 0
CUI: C0016529
Disease: Forced expiratory volume function
Forced expiratory volume function 		272 0 1 2.6E-03 0 0
CUI: C0027066
Disease: Myoclonus
Myoclonus 		265 0 1 2.6E-03 0 0
CUI: C0266435
Disease: Congenital hypoplasia of penis
Congenital hypoplasia of penis 		237 0 1 2.8E-03 0 0
CUI: C1306503
Disease: Congenital exomphalos
Congenital exomphalos 		235 0 1 2.9E-03 0 0
CUI: C1854882
Disease: Absent speech
Absent speech 		232 0 1 2.9E-03 0 0