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: C0271738
Disease: Hypocortisolism secondary to another disorder
Hypocortisolism secondary to another disorder 		13 0 3 0.12 0 0
CUI: C0155552
Disease: Hearing Loss, Mixed Conductive-Sensorineural
Hearing Loss, Mixed Conductive-Sensorineural 		23 0 4 0.11 0 0
CUI: C0265857
Disease: Uhl anomaly
Uhl anomaly 		4 0 2 0.11 0 0
CUI: C1849538
Disease: Delayed eruption of primary teeth
Delayed eruption of primary teeth 		14 0 3 0.11 0 0
CUI: C3553368
Disease: Limited hip extension
Limited hip extension 		4 0 2 0.11 0 0
CUI: C4021723
Disease: Short middle phalanx of toe
Short middle phalanx of toe 		4 0 2 0.11 0 0
CUI: C4082954
Disease: Hypoplasia of right ventricle
Hypoplasia of right ventricle 		4 0 2 0.11 0 0
CUI: C0846967
Disease: Acanthoma
Acanthoma 		5 0 2 0.11 0 0
CUI: C1848587
Disease: Isolated hypoplasia of the right ventricle
Isolated hypoplasia of the right ventricle 		5 0 2 0.11 0 0
CUI: C2676443
Disease: Proximal radio-ulnar synostosis
Proximal radio-ulnar synostosis 		5 0 2 0.11 0 0
CUI: C0235857
Disease: Decreased lacrimation
Decreased lacrimation 		6 0 2 1.0E-01 0 0
CUI: C0271742
Disease: Glucocorticoid deficiency with achalasia
Glucocorticoid deficiency with achalasia 		17 20 3 1.0E-01 1 5.0E-02
CUI: C0406803
Disease: Syringocystadenoma Papilliferum
Syringocystadenoma Papilliferum 		6 0 2 1.0E-01 0 0
CUI: C4021164
Disease: Bicoronal synostosis
Bicoronal synostosis 		6 0 2 1.0E-01 0 0
CUI: C4021395
Disease: Abnormality of the antihelix
Abnormality of the antihelix 		17 0 3 1.0E-01 0 0
CUI: C1561989
Disease: Limbal stem cell deficiency
Limbal stem cell deficiency 		19 0 3 9.4E-02 0 0
CUI: C0001193
Disease: Apert syndrome
Apert syndrome 		20 0 3 9.1E-02 0 0
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		8 0 2 9.1E-02 0 0
CUI: C0948387
Disease: Secondary Adrenal Insufficiency
Secondary Adrenal Insufficiency 		20 0 3 9.1E-02 0 0
CUI: C1860050
Disease: Cloverleaf skull
Cloverleaf skull 		8 0 2 9.1E-02 0 0
CUI: C0149801
Disease: Sepsis due to urinary tract infection
Sepsis due to urinary tract infection 		9 0 2 8.7E-02 0 0
CUI: C0340766
Disease: Venous hypertension
Venous hypertension 		9 0 2 8.7E-02 0 0
CUI: C0456107
Disease: Neonatal meningitis
Neonatal meningitis 		9 0 2 8.7E-02 0 0
CUI: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature 		9 0 2 8.7E-02 0 0
CUI: C4054695
Disease: Familial glucocorticoid deficiency
Familial glucocorticoid deficiency 		9 0 2 8.7E-02 0 0