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: C0271271
Disease: Xerotic keratitis
Xerotic keratitis 		1 0 1 0.50 0 0
CUI: C0341702
Disease: Acquired Fanconi syndrome
Acquired Fanconi syndrome 		1 0 1 0.50 0 0
CUI: C0406481
Disease: Comedonal acne
Comedonal acne 		2 0 1 0.33 0 0
CUI: C3553016
Disease: Peripheral retinal atrophy
Peripheral retinal atrophy 		2 0 1 0.33 0 0
CUI: C3554593
Disease: RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME
RETINAL DYSTROPHY, IRIS COLOBOMA, AND COMEDOGENIC ACNE SYNDROME 		2 0 1 0.33 0 0
CUI: C4225330
Disease: MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10
MICROPHTHALMIA, ISOLATED, WITH COLOBOMA 10 		2 0 1 0.33 0 0
CUI: C0162279
Disease: Choroidal detachment
Choroidal detachment 		3 0 1 0.25 0 0
CUI: C0206247
Disease: Amyloid Neuropathies
Amyloid Neuropathies 		3 0 1 0.25 0 0
CUI: C0856901
Disease: Retinol Deficiency
Retinol Deficiency 		3 0 1 0.25 0 0
CUI: C4531196
Disease: Transthyretin cardiac amyloidosis
Transthyretin cardiac amyloidosis 		3 0 1 0.25 0 0
CUI: C0021296
Disease: Infant, Small for Gestational Age
Infant, Small for Gestational Age 		4 0 1 0.20 0 0
CUI: C0268465
Disease: Phenylketonuria II
Phenylketonuria II 		6 0 1 0.14 0 0
CUI: C2931501
Disease: Microphthalmia associated with colobomatous cyst
Microphthalmia associated with colobomatous cyst 		8 0 1 0.11 0 0
CUI: C0023176
Disease: Lead Poisoning
Lead Poisoning 		9 0 1 1.0E-01 0 0
CUI: C0751436
Disease: Hyperphenylalaninemia, Non-Phenylketonuric
Hyperphenylalaninemia, Non-Phenylketonuric 		9 0 1 1.0E-01 0 0
CUI: C0856151
Disease: Fat redistribution
Fat redistribution 		12 0 1 7.7E-02 0 0
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
Amyloid Neuropathies, Familial 		15 0 1 6.2E-02 0 0
CUI: C2316786
Disease: Chronic kidney disease stage 2
Chronic kidney disease stage 2 		15 0 1 6.2E-02 0 0
CUI: C4022459
Disease: Decreased adipose tissue
Decreased adipose tissue 		17 0 1 5.6E-02 0 0
CUI: C0004782
Disease: Basal Ganglia Diseases
Basal Ganglia Diseases 		19 0 1 5.0E-02 0 0
CUI: C0085399
Disease: Ehrlichiosis
Ehrlichiosis 		21 0 1 4.5E-02 0 0
CUI: C0878681
Disease: Dent's disease
Dent's disease 		23 0 1 4.2E-02 0 0
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome 		25 0 1 3.8E-02 0 0
CUI: C0282548
Disease: Leukostasis
Leukostasis 		25 0 1 3.8E-02 0 0
CUI: C0017097
Disease: Gardner Syndrome
Gardner Syndrome 		29 0 1 3.3E-02 0 0