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: C4024819
Disease: Abnormality of chorioretinal pigmentation
Abnormality of chorioretinal pigmentation 		1 0 1 1.7E-02 0 0
CUI: C4087521
Disease: Adjacent segment disease
Adjacent segment disease 		1 0 1 1.7E-02 0 0
CUI: C4255215
Disease: Dysplastic tricuspid valve
Dysplastic tricuspid valve 		1 0 1 1.7E-02 0 0
CUI: C4310685
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 47 		1 0 1 1.7E-02 0 0
CUI: C4693985
Disease: EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 1
EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 1 		1 0 1 1.7E-02 0 0
CUI: C4748334
Disease: DEAFNESS, AUTOSOMAL DOMINANT 74
DEAFNESS, AUTOSOMAL DOMINANT 74 		1 0 1 1.7E-02 0 0
CUI: C4748952
Disease: Hepatopulmonary fusion
Hepatopulmonary fusion 		1 0 1 1.7E-02 0 0
CUI: C0036400
Disease: Scimitar Syndrome
Scimitar Syndrome 		2 0 2 3.4E-02 0 0
CUI: C0036913
Disease: Sexual Sadism
Sexual Sadism 		2 0 1 1.7E-02 0 0
CUI: C0086774
Disease: Cold paroxysmal hemoglobinuria
Cold paroxysmal hemoglobinuria 		2 0 1 1.7E-02 0 0
CUI: C0153562
Disease: Kaposi's sarcoma of palate
Kaposi's sarcoma of palate 		2 0 1 1.7E-02 0 0
CUI: C0154733
Disease: Multiple cranial nerve palsy
Multiple cranial nerve palsy 		2 0 1 1.7E-02 0 0
CUI: C0271004
Disease: Absent anterior chamber of eye
Absent anterior chamber of eye 		2 0 1 1.7E-02 0 0
CUI: C0311213
Disease: Dermatitis verrucosa
Dermatitis verrucosa 		2 0 1 1.7E-02 0 0
CUI: C0339491
Disease: Sickle cell retinopathy
Sickle cell retinopathy 		2 0 1 1.7E-02 0 0
CUI: C0426317
Disease: Genitourinary symptoms
Genitourinary symptoms 		2 0 1 1.7E-02 0 0
CUI: C0561843
Disease: Memory, Episodic
Memory, Episodic 		2 0 1 1.7E-02 0 0
CUI: C0679499
Disease: sexual deviance
sexual deviance 		2 0 1 1.7E-02 0 0
CUI: C0854440
Disease: Fatty acid deficiency
Fatty acid deficiency 		2 0 1 1.7E-02 0 0
CUI: C0948825
Disease: Systremma
Systremma 		2 0 1 1.7E-02 0 0
CUI: C1735593
Disease: Intracardiac mass
Intracardiac mass 		2 0 1 1.7E-02 0 0
CUI: C1735886
Disease: Bland White Garland Syndrome
Bland White Garland Syndrome 		2 0 2 3.4E-02 0 0
CUI: C1838502
Disease: NANOPHTHALMOS 1
NANOPHTHALMOS 1 		2 0 1 1.7E-02 0 0
CUI: C1848029
Disease: Ehlers-Danlos syndrome caused by tenascin-X deficiency
Ehlers-Danlos syndrome caused by tenascin-X deficiency 		2 0 1 1.7E-02 0 0
CUI: C1851316
Disease: Iron Overload, Autosomal Dominant
Iron Overload, Autosomal Dominant 		2 0 1 1.7E-02 0 0