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: C1836946
Disease: Peripheral Cone Dystrophy
Peripheral Cone Dystrophy 		1 0 1 1.00 0 0
CUI: C0302129
Disease: Achromatopsia 1
Achromatopsia 1 		20 0 1 5.0E-02 0 0
CUI: C0403553
Disease: Renal dysplasia and retinal aplasia (disorder)
Renal dysplasia and retinal aplasia (disorder) 		20 0 1 5.0E-02 0 0
CUI: C0152200
Disease: Achromatopsia
Achromatopsia 		26 0 1 3.8E-02 0 0
CUI: C0036346
Disease: Schizophrenia, Childhood
Schizophrenia, Childhood 		33 0 1 3.0E-02 0 0
CUI: C0152191
Disease: Scotoma, Central
Scotoma, Central 		43 0 1 2.3E-02 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 31 1 2.1E-02 1 3.0E-02
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 1.8E-02 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		63 2 1 1.6E-02 1 0.25
CUI: C1859308
Disease: PREMATURE CENTROMERE DIVISION
PREMATURE CENTROMERE DIVISION 		66 0 1 1.5E-02 0 0
CUI: C2931258
Disease: Amaurosis congenita of Leber, type 1
Amaurosis congenita of Leber, type 1 		81 0 1 1.2E-02 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 53 1 1.2E-02 1 1.8E-02
CUI: C0022679
Disease: Cystic kidney
Cystic kidney 		89 0 1 1.1E-02 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 1.1E-02 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 1.1E-02 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure 		109 0 1 9.2E-03 0 0
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure 		139 0 1 7.2E-03 0 0
CUI: C0750880
Disease: Monocyte count result
Monocyte count result 		139 0 1 7.2E-03 0 0
CUI: C0428886
Disease: Mean blood pressure
Mean blood pressure 		146 0 1 6.8E-03 0 0
CUI: C0234632
Disease: Reduced visual acuity
Reduced visual acuity 		147 0 1 6.8E-03 0 0
CUI: C4552000
Disease: Episodic Kinesigenic Dyskinesia 1
Episodic Kinesigenic Dyskinesia 1 		153 0 1 6.5E-03 0 0
CUI: C4551563
Disease: Microcephaly (physical finding)
Microcephaly (physical finding) 		160 246 1 6.3E-03 1 4.0E-03
CUI: C4551720
Disease: Primary Ciliary Dyskinesia
Primary Ciliary Dyskinesia 		160 0 1 6.3E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 6.0E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		194 33 1 5.2E-03 1 2.9E-02