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: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 2 3.9E-02
CUI: C1862591
Disease: CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 2.3E-02
CUI: C3809971
Disease: ASPARAGINE SYNTHETASE DEFICIENCY
ASPARAGINE SYNTHETASE DEFICIENCY 		0 13 0 0 1 1.8E-02
CUI: C3899405
Disease: Decreased Attention
Decreased Attention 		0 3 0 0 1 2.2E-02
CUI: C4021813
Disease: Oral cleft
Oral cleft 		85 0 1 1.9E-03 0 0
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		83 0 1 1.9E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.9E-03 0 0
CUI: C0406810
Disease: Carney Complex
Carney Complex 		82 0 1 1.9E-03 0 0
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		82 0 1 1.9E-03 0 0
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		82 0 1 1.9E-03 0 0
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		82 0 1 1.9E-03 0 0
CUI: C0206693
Disease: Medullary carcinoma
Medullary carcinoma 		81 0 1 1.9E-03 0 0
CUI: C0040588
Disease: Tracheoesophageal Fistula
Tracheoesophageal Fistula 		80 0 1 1.9E-03 0 0
CUI: C2936904
Disease: Opitz GBBB Syndrome, X-Linked
Opitz GBBB Syndrome, X-Linked 		79 0 1 1.9E-03 0 0
CUI: C0429028
Disease: QT interval feature (observable entity)
QT interval feature (observable entity) 		75 0 1 1.9E-03 0 0
CUI: C0221263
Disease: Cafe-au-Lait Spots
Cafe-au-Lait Spots 		74 0 1 1.9E-03 0 0
CUI: C4023106
Disease: Obstructive azoospermia
Obstructive azoospermia 		74 0 1 1.9E-03 0 0
CUI: C0242343
Disease: Panhypopituitarism
Panhypopituitarism 		73 0 1 1.9E-03 0 0
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome 		71 0 1 1.9E-03 0 0
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		70 0 1 1.9E-03 0 0
CUI: C1859592
Disease: ATRICHIA WITH PAPULAR LESIONS
ATRICHIA WITH PAPULAR LESIONS 		70 0 1 1.9E-03 0 0
CUI: C1963099
Disease: Myelodysplasia, CTCAE
Myelodysplasia, CTCAE 		68 0 1 1.9E-03 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 1.9E-03 0 0
CUI: C0035227
Disease: Respiratory Function Tests
Respiratory Function Tests 		67 0 1 1.9E-03 0 0
CUI: C0158761
Disease: Radioulnar Synostosis
Radioulnar Synostosis 		67 0 1 1.9E-03 0 0