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: C1846529
Disease: CONE-ROD DYSTROPHY 10
CONE-ROD DYSTROPHY 10 		1 2 1 1.00 2 1.00
CUI: C0206615
Disease: Pneumovirus Infections
Pneumovirus Infections 		3 0 1 0.33 0 0
CUI: C3896578
Disease: Familial Colorectal Cancer Type X
Familial Colorectal Cancer Type X 		14 0 1 7.1E-02 0 0
CUI: C4020965
Disease: Cardiac diverticulum
Cardiac diverticulum 		14 0 1 7.1E-02 0 0
CUI: C0001816
Disease: Agnosia
Agnosia 		17 0 1 5.9E-02 0 0
CUI: C2732838
Disease: Neoplasm of skeletal system
Neoplasm of skeletal system 		17 0 1 5.9E-02 0 0
CUI: C0241688
Disease: Peripheral visual field loss
Peripheral visual field loss 		19 0 1 5.3E-02 0 0
CUI: C0347509
Disease: Benign neoplasm of central nervous system
Benign neoplasm of central nervous system 		21 0 1 4.8E-02 0 0
CUI: C1333991
Disease: Hereditary Non-Polyposis Colon Cancer Type 2
Hereditary Non-Polyposis Colon Cancer Type 2 		23 0 1 4.3E-02 0 0
CUI: C2936783
Disease: Colorectal cancer, hereditary nonpolyposis, type 1
Colorectal cancer, hereditary nonpolyposis, type 1 		24 0 1 4.2E-02 0 0
CUI: C0152227
Disease: Excessive tearing
Excessive tearing 		26 0 1 3.8E-02 0 0
CUI: C0042076
Disease: Urologic Neoplasms
Urologic Neoplasms 		28 0 1 3.6E-02 0 0
CUI: C1112155
Disease: Hereditary non-polyposis colorectal cancer syndrome
Hereditary non-polyposis colorectal cancer syndrome 		31 0 1 3.2E-02 0 0
CUI: C0042138
Disease: Uterine Neoplasms
Uterine Neoplasms 		32 0 1 3.1E-02 0 0
CUI: C0009405
Disease: Hereditary Nonpolyposis Colorectal Neoplasms
Hereditary Nonpolyposis Colorectal Neoplasms 		40 0 1 2.5E-02 0 0
CUI: C0234144
Disease: Dysgraphia
Dysgraphia 		43 0 1 2.3E-02 0 0
CUI: C1536999
Disease: cancer angiogenesis
cancer angiogenesis 		44 0 1 2.3E-02 0 0
CUI: C3887875
Disease: Visual field defects
Visual field defects 		47 0 1 2.1E-02 0 0
CUI: C0149793
Disease: Amaurosis Fugax
Amaurosis Fugax 		49 0 1 2.0E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation 		58 0 1 1.7E-02 0 0
CUI: C0151740
Disease: Intracranial Hypertension
Intracranial Hypertension 		72 0 1 1.4E-02 0 0
CUI: C1839364
Disease: Progressive visual loss
Progressive visual loss 		77 0 1 1.3E-02 0 0
CUI: C0339525
Disease: Autosomal dominant retinitis pigmentosa
Autosomal dominant retinitis pigmentosa 		85 0 1 1.2E-02 0 0
CUI: C4085590
Disease: Cone-Rod Dystrophies
Cone-Rod Dystrophies 		86 0 1 1.2E-02 0 0
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 1.1E-02 0 0