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: C0341702
Disease: Acquired Fanconi syndrome
Acquired Fanconi syndrome 		1 0 1 1.00 0 0
CUI: C0152455
Disease: Keratomalacia
Keratomalacia 		2 0 1 0.50 0 0
CUI: C0406481
Disease: Comedonal acne
Comedonal acne 		2 0 1 0.50 0 0
CUI: C3553016
Disease: Peripheral retinal atrophy
Peripheral retinal atrophy 		2 0 1 0.50 0 0
CUI: C3554593
Disease: RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME
RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME 		2 0 1 0.50 0 0
CUI: C4225330
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10 		2 0 1 0.50 0 0
CUI: C0162279
Disease: Choroidal detachment
Choroidal detachment 		3 0 1 0.33 0 0
CUI: C0206247
Disease: Amyloid Neuropathies
Amyloid Neuropathies 		3 0 1 0.33 0 0
CUI: C0856901
Disease: Retinol Deficiency
Retinol Deficiency 		3 0 1 0.33 0 0
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
Transthyretin cardiac amyloidosis 		3 0 1 0.33 0 0
CUI: C0021296
Disease: Infant, Small for Gestational Age
Infant, Small for Gestational Age 		4 0 1 0.25 0 0
CUI: C2931501
Disease: Microphthalmia associated with colobomatous cyst
Microphthalmia associated with colobomatous cyst 		8 0 1 0.12 0 0
CUI: C0856151
Disease: Fat redistribution
Fat redistribution 		12 0 1 8.3E-02 0 0
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
Amyloid Neuropathies, Familial 		15 0 1 6.7E-02 0 0
CUI: C2316786
Disease: Chronic kidney disease stage 2
Chronic kidney disease stage 2 		15 0 1 6.7E-02 0 0
CUI: C4022459
Disease: Decreased adipose tissue
Decreased adipose tissue 		17 0 1 5.9E-02 0 0
CUI: C0085399
Disease: Ehrlichiosis
Ehrlichiosis 		21 0 1 4.8E-02 0 0
CUI: C0878681
Disease: Dent's disease
Dent's disease 		23 0 1 4.3E-02 0 0
CUI: C0282548
Disease: Leukostasis
Leukostasis 		25 0 1 4.0E-02 0 0
CUI: C0017097
Disease: Gardner Syndrome
Gardner Syndrome 		29 0 1 3.4E-02 0 0
CUI: C0235272
Disease: Retinal damage
Retinal damage 		32 0 1 3.1E-02 0 0
CUI: C0339535
Disease: Night blindness, congenital stationary
Night blindness, congenital stationary 		32 0 1 3.1E-02 0 0
CUI: C0268407
Disease: Senile cardiac amyloidosis
Senile cardiac amyloidosis 		33 0 1 3.0E-02 0 0
CUI: C0271790
Disease: Subclinical hypothyroidism
Subclinical hypothyroidism 		40 0 1 2.5E-02 0 0
CUI: C0271093
Disease: Stargardt's disease
Stargardt's disease 		45 0 1 2.2E-02 0 0