Source: CTD_human

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C3280099
Disease: CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME
CRANIOFACIAL ANOMALIES AND ANTERIOR SEGMENT DYSGENESIS SYNDROME 		disease 0.700 moderate 1.000 0 0 2004 2004
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C1835677
Disease: Keratoconus 1
Keratoconus 1 		disease 0.700 None 1.000 0 0 2002 2011
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0022578
Disease: Keratoconus
Keratoconus 		disease 0.500 None 0.871 2 0 2002 2019
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0376634
Disease: Craniofacial Abnormalities
Craniofacial Abnormalities 		group 0.320 None 1.000 1 0 2004 2012
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0751097
Disease: Empty Sella Syndrome, Secondary
Empty Sella Syndrome, Secondary 		disease 0.300 None 1.000 1 0 2004 2004
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0750942
Disease: Auditory Inattention
Auditory Inattention 		phenotype 0.300 None 1.000 1 0 2004 2004
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0271574
Disease: Empty Sella Syndrome, Primary
Empty Sella Syndrome, Primary 		disease 0.300 None 1.000 1 0 2004 2004
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0038457
Disease: Stromal Dystrophies, Corneal
Stromal Dystrophies, Corneal 		group 0.300 None 1.000 1 0 2002 2002
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0035309
Disease: Retinal Diseases
Retinal Diseases 		group 0.300 None 1.000 1 0 2004 2004
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0024439
Disease: Macular corneal dystrophy
Macular corneal dystrophy 		disease 0.300 None 1.000 1 0 2002 2002
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0018245
Disease: Groenouw's Dystrophies
Groenouw's Dystrophies 		disease 0.300 None 1.000 1 0 2002 2002
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0018179
Disease: Granular Dystrophy, Corneal
Granular Dystrophy, Corneal 		disease 0.300 None 1.000 1 0 2002 2002
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0015393
Disease: Eye Abnormalities
Eye Abnormalities 		group 0.300 None 1.000 1 0 2004 2004
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0014008
Disease: Empty Sella Syndrome
Empty Sella Syndrome 		disease 0.300 None 1.000 1 0 2004 2004
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0010035
Disease: Hereditary corneal dystrophy
Hereditary corneal dystrophy 		disease 0.300 None 1.000 1 0 2002 2002
Entrez Id: 30813
Gene Symbol: VSX1
VSX1 		visual system homeobox 1 0.579 0.692 3.6E-02
CUI: C0004310
Disease: Auditory Perceptual Disorders
Auditory Perceptual Disorders 		group 0.300 None 1.000 1 0 2004 2004