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: C0751161
Disease: UDPglucose 4-epimerase deficiency disease
UDPglucose 4-epimerase deficiency disease 		3 0 2 0.22 0 0
CUI: C4021643
Disease: Impairment of galactose metabolism
Impairment of galactose metabolism 		3 0 2 0.22 0 0
CUI: C0268157
Disease: Galactosuria
Galactosuria 		4 0 2 0.20 0 0
CUI: C4023071
Disease: Hypergalactosemia
Hypergalactosemia 		4 0 2 0.20 0 0
CUI: C0152259
Disease: Cataract secondary to ocular disorder
Cataract secondary to ocular disorder 		5 0 2 0.18 0 0
CUI: C4721766
Disease: Unspecified secondary cataract
Unspecified secondary cataract 		5 0 2 0.18 0 0
CUI: C0268155
Disease: Deficiency of galactokinase
Deficiency of galactokinase 		6 0 2 0.17 0 0
CUI: C0152112
Disease: Foster-Kennedy Syndrome
Foster-Kennedy Syndrome 		1 0 1 0.12 0 0
CUI: C0268152
Disease: Classical galactosemia, homozygous Duarte-type
Classical galactosemia, homozygous Duarte-type 		1 0 1 0.12 0 0
CUI: C0271149
Disease: Secondary angle-closure glaucoma
Secondary angle-closure glaucoma 		1 0 1 0.12 0 0
CUI: C0271152
Disease: Malignant glaucoma
Malignant glaucoma 		1 0 1 0.12 0 0
CUI: C0342745
Disease: Disorder of galactose metabolism
Disorder of galactose metabolism 		1 0 1 0.12 0 0
CUI: C0398641
Disease: Epstein syndrome (disorder)
Epstein syndrome (disorder) 		1 0 1 0.12 0 0
CUI: C0403445
Disease: Fechtner syndrome (disorder)
Fechtner syndrome (disorder) 		1 0 1 0.12 0 0
CUI: C0563632
Disease: Manifest-latent nystagmus
Manifest-latent nystagmus 		1 0 1 0.12 0 0
CUI: C0751402
Disease: Optic Disk Disorders
Optic Disk Disorders 		1 0 1 0.12 0 0
CUI: C0751535
Disease: Syncope, Cardiogenic
Syncope, Cardiogenic 		1 0 1 0.12 0 0
CUI: C1261251
Disease: Agenesis of vagina
Agenesis of vagina 		1 0 1 0.12 0 0
CUI: C1300202
Disease: Diaphyseal medullary stenosis with bone malignancy
Diaphyseal medullary stenosis with bone malignancy 		1 0 1 0.12 0 0
CUI: C1720732
Disease: Subretinal fluid (finding)
Subretinal fluid (finding) 		1 0 1 0.12 0 0
CUI: C1834478
Disease: MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS
MACROTHROMBOCYTOPENIA AND PROGRESSIVE SENSORINEURAL DEAFNESS 		1 0 1 0.12 0 0
CUI: C1842035
Disease: Giant Platelet Syndrome with Thrombocytopenia
Giant Platelet Syndrome with Thrombocytopenia 		1 0 1 0.12 0 0
CUI: C1861512
Disease: Cochleosaccular degeneration of the inner ear and progressive cataracts
Cochleosaccular degeneration of the inner ear and progressive cataracts 		1 0 1 0.12 0 0
CUI: C1863659
Disease: DEAFNESS, AUTOSOMAL DOMINANT 17
DEAFNESS, AUTOSOMAL DOMINANT 17 		1 0 1 0.12 0 0
CUI: C2315667
Disease: Fetal microcephaly
Fetal microcephaly 		1 0 1 0.12 0 0