Source: INFERRED

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: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C3150819
Disease: RETINITIS PIGMENTOSA 56
RETINITIS PIGMENTOSA 56 		disease 0.600 None 0 5
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C4015343
Disease: MACULAR DYSTROPHY, VITELLIFORM, 5
MACULAR DYSTROPHY, VITELLIFORM, 5 		disease 0.600 limited 1.000 0 4 2010 2017
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		disease 0.420 strong 1.000 0 8 2010 2014
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration 		disease 0.110 None 1.000 0 0 2001 2001
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies 		group 0.100 None 1.000 1 4 2010 2010
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy 		disease 0.100 None 1.000 1 1 2019 2019
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye 		phenotype 0.100 None 1.000 1 1 2010 2010
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		disease 0.100 None 1.000 1 1 2017 2017
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		group 0.100 None 1.000 1 1 2017 2017
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C1840077
Disease: Anteverted nostril
Anteverted nostril 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0858617
Disease: Posterior subcapsular cataract
Posterior subcapsular cataract 		disease 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0085636
Disease: Photophobia
Photophobia 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C1849367
Disease: Nasal bridge wide
Nasal bridge wide 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C1963184
Disease: Nystagmus, CTCAE 3.0
Nystagmus, CTCAE 3.0 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy 		disease 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C4024817
Disease: Vitelliform-like macular lesions
Vitelliform-like macular lesions 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C4021563
Disease: Retinal nonattachment
Retinal nonattachment 		disease 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C3887875
Disease: Visual field defects
Visual field defects 		group 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability 		group 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C4554036
Disease: Nystagmus, CTCAE 5.0
Nystagmus, CTCAE 5.0 		phenotype 0.100 None 0 0
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2 		interphotoreceptor matrix proteoglycan 2 0.659 0.308 2.8E-13
CUI: C0456909
Disease: Blindness
Blindness 		phenotype 0.100 None 0 0