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: C0339682
Disease: Regular astigmatism - corneal
Regular astigmatism - corneal 		34 28 2 2.8E-02 1 8.0E-03
CUI: C1859726
Disease: ARTERIAL TORTUOSITY SYNDROME
ARTERIAL TORTUOSITY SYNDROME 		37 0 2 2.7E-02 0 0
CUI: C1821417
Disease: RESTING HEART RATE
RESTING HEART RATE 		80 0 3 2.6E-02 0 0
CUI: C0152207
Disease: Alternating Exotropia
Alternating Exotropia 		1 0 1 2.6E-02 0 0
CUI: C0155116
Disease: Descemet's membrane fold
Descemet's membrane fold 		1 0 1 2.6E-02 0 0
CUI: C0334113
Disease: Eosinophilic granulomatous polyp
Eosinophilic granulomatous polyp 		1 0 1 2.6E-02 0 0
CUI: C0474441
Disease: Fine corneal edema
Fine corneal edema 		1 0 1 2.6E-02 0 0
CUI: C0549651
Disease: Abnormality of the lens
Abnormality of the lens 		1 0 1 2.6E-02 0 0
CUI: C0948384
Disease: Cerebral hygroma
Cerebral hygroma 		1 0 1 2.6E-02 0 0
CUI: C1510410
Disease: Sense of smell altered
Sense of smell altered 		1 0 1 2.6E-02 0 0
CUI: C1842357
Disease: Slowed Nerve Conduction Velocity, Autosomal Dominant
Slowed Nerve Conduction Velocity, Autosomal Dominant 		1 0 1 2.6E-02 0 0
CUI: C1845109
Disease: Exaggerated median tongue furrow
Exaggerated median tongue furrow 		1 0 1 2.6E-02 0 0
CUI: C1852795
Disease: CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2 		1 0 1 2.6E-02 0 0
CUI: C1855188
Disease: Metaphyseal Chondrodysplasia with Retinitis Pigmentosa
Metaphyseal Chondrodysplasia with Retinitis Pigmentosa 		1 0 1 2.6E-02 0 0
CUI: C1868000
Disease: Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal
Polyps, Multiple And Recurrent Inflammatory Fibroid, Gastrointestinal 		1 0 1 2.6E-02 0 0
CUI: C2825916
Disease: Vascular Cell Adhesion Molecule 1 Measurement
Vascular Cell Adhesion Molecule 1 Measurement 		1 0 1 2.6E-02 0 0
CUI: C3151087
Disease: LOEYS-DIETZ SYNDROME 3
LOEYS-DIETZ SYNDROME 3 		1 0 1 2.6E-02 0 0
CUI: C3554665
Disease: OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA
OSTEOSCLEROTIC METAPHYSEAL DYSPLASIA 		1 0 1 2.6E-02 0 0
CUI: C3715216
Disease: RETINITIS PIGMENTOSA 66
RETINITIS PIGMENTOSA 66 		1 0 1 2.6E-02 0 0
CUI: C3806616
Disease: Macular hypopigmented whorls, streaks, and patches
Macular hypopigmented whorls, streaks, and patches 		1 0 1 2.6E-02 0 0
CUI: C4016331
Disease: HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC, RESISTANT TO IMATINIB
HYPEREOSINOPHILIC SYNDROME, IDIOPATHIC, RESISTANT TO IMATINIB 		1 0 1 2.6E-02 0 0
CUI: C4022133
Disease: Tibial deviation of the 5th toe
Tibial deviation of the 5th toe 		1 0 1 2.6E-02 0 0
CUI: C4022135
Disease: Tibial deviation of the 2nd toe
Tibial deviation of the 2nd toe 		1 0 1 2.6E-02 0 0
CUI: C4024137
Disease: Partial duplication of the proximal phalanx of the 3rd finger
Partial duplication of the proximal phalanx of the 3rd finger 		1 0 1 2.6E-02 0 0
CUI: C4024140
Disease: Complete duplication of the middle phalanx of the 3rd finger
Complete duplication of the middle phalanx of the 3rd finger 		1 0 1 2.6E-02 0 0