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: C4025327
Disease: Congenital pyloric atresia
Congenital pyloric atresia 		6 0 3 0.10 0 0
CUI: C0221260
Disease: Dystrophia unguium
Dystrophia unguium 		81 0 10 0.10 0 0
CUI: C1290344
Disease: Nonspecific interstitial pneumonia
Nonspecific interstitial pneumonia 		28 0 5 0.10 0 0
CUI: C3489393
Disease: Hiatal Hernia
Hiatal Hernia 		39 0 6 0.10 0 0
CUI: C0079299
Disease: Epidermolysis Bullosa Simplex Kobner
Epidermolysis Bullosa Simplex Kobner 		7 28 3 1.0E-01 3 1.0E-01
CUI: C0266159
Disease: Pyloric Atresia
Pyloric Atresia 		7 0 3 1.0E-01 0 0
CUI: C0268338
Disease: Ehlers-Danlos Syndrome, Type IV
Ehlers-Danlos Syndrome, Type IV 		7 0 3 1.0E-01 0 0
CUI: C1844738
Disease: Axillary pterygium
Axillary pterygium 		7 0 3 1.0E-01 0 0
CUI: C1856934
Disease: Epidermolysis bullosa with pyloric atresia
Epidermolysis bullosa with pyloric atresia 		7 0 3 1.0E-01 0 0
CUI: C1969236
Disease: Mitten deformity
Mitten deformity 		7 0 3 1.0E-01 0 0
CUI: C0265998
Disease: ANONYCHIA
ANONYCHIA 		30 0 5 9.8E-02 0 0
CUI: C0432363
Disease: Shagreen patch
Shagreen patch 		8 0 3 9.7E-02 0 0
CUI: C0575484
Disease: Long thorax
Long thorax 		9 0 3 9.4E-02 0 0
CUI: C3887531
Disease: Keratoglobus
Keratoglobus 		9 0 3 9.4E-02 0 0
CUI: C0542514
Disease: Blue sclera
Blue sclera 		70 0 8 9.1E-02 0 0
CUI: C0856747
Disease: Aneurysm of ascending aorta
Aneurysm of ascending aorta 		34 0 5 9.1E-02 0 0
CUI: C1833762
Disease: Decreased calvarial ossification
Decreased calvarial ossification 		10 0 3 9.1E-02 0 0
CUI: C1858732
Disease: Malar prominence
Malar prominence 		10 0 3 9.1E-02 0 0
CUI: C0013592
Disease: Ectropion
Ectropion 		50 0 6 8.6E-02 0 0
CUI: C0013720
Disease: Ehlers-Danlos Syndrome
Ehlers-Danlos Syndrome 		77 14 8 8.4E-02 1 5.6E-02
CUI: C0040962
Disease: Tricuspid Valve Prolapse
Tricuspid Valve Prolapse 		13 0 3 8.3E-02 0 0
CUI: C0743178
Disease: Intractable diarrhea
Intractable diarrhea 		13 0 3 8.3E-02 0 0
CUI: C4021816
Disease: Abnormality of the gingiva
Abnormality of the gingiva 		13 0 3 8.3E-02 0 0
CUI: C1846545
Disease: Autoimmune Lymphoproliferative Syndrome Type 2B
Autoimmune Lymphoproliferative Syndrome Type 2B 		14 2 3 8.1E-02 1 0.17
CUI: C4021986
Disease: Hypoplasia of the ear cartilage
Hypoplasia of the ear cartilage 		14 0 3 8.1E-02 0 0