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: C1859773
Disease: Microphthalmia, Syndromic 3
Microphthalmia, Syndromic 3
5 0 2 0.20 0 0
CUI: C1855052
Disease: MICROPHTHALMIA, ISOLATED 1
MICROPHTHALMIA, ISOLATED 1
8 0 2 0.15 0 0
CUI: C4551977
Disease: Microphthalmos, Autosomal Recessive
Microphthalmos, Autosomal Recessive
8 0 2 0.15 0 0
CUI: C0033075
Disease: Presbyopia
Presbyopia
1 1 1 0.14 1 0.50
Familial amyloid polyneuropathy, type VI
1 0 1 0.14 0 0
Familial Amyloid Polyneuropathy, Jewish Type
1 0 1 0.14 0 0
CUI: C0268386
Disease: Amyloid Polyneuropathy, Swiss Type
Amyloid Polyneuropathy, Swiss Type
1 0 1 0.14 0 0
CUI: C0339562
Disease: Amyloid of vitreous
Amyloid of vitreous
1 1 1 0.14 1 0.50
Amyloid Polyneuropathy, British Type (disorder)
1 0 1 0.14 0 0
CUI: C0343287
Disease: Thoracic discitis
Thoracic discitis
1 0 1 0.14 0 0
CUI: C0423463
Disease: Opticociliary vessels
Opticociliary vessels
1 0 1 0.14 0 0
CUI: C0546394
Disease: Nodular cutaneous amyloidosis
Nodular cutaneous amyloidosis
1 0 1 0.14 0 0
CUI: C0570855
Disease: Allergy to chlorpromazine
Allergy to chlorpromazine
1 0 1 0.14 0 0
CUI: C0700376
Disease: Pulmonary amyloidosis
Pulmonary amyloidosis
1 0 1 0.14 0 0
CUI: C0741918
Disease: Structural cardiac defects
Structural cardiac defects
1 0 1 0.14 0 0
CUI: C1266176
Disease: Atypical choroid plexus papilloma
Atypical choroid plexus papilloma
1 0 1 0.14 0 0
CUI: C1321315
Disease: Paraneoplastic retinopathy
Paraneoplastic retinopathy
1 0 1 0.14 0 0
CUI: C1333100
Disease: Squamous cell carcinoma of colon
Squamous cell carcinoma of colon
1 0 1 0.14 0 0
Familial Amyloid Polyneuropathy, Appalachian Type
1 0 1 0.14 0 0
CUI: C1846266
Disease: Laterally curved eyebrow
Laterally curved eyebrow
1 0 1 0.14 0 0
CUI: C1849164
Disease: Long, smooth philtrum
Long, smooth philtrum
1 0 1 0.14 0 0
CUI: C1855286
Disease: Long curly eyelashes
Long curly eyelashes
1 0 1 0.14 0 0
CUI: C1864690
Disease: Microphthalmia, Syndromic 5
Microphthalmia, Syndromic 5
1 0 1 0.14 0 0
NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C
1 0 1 0.14 0 0
Chromosome 5p13 Duplication Syndrome
1 0 1 0.14 0 0