Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C3150819
Disease: RETINITIS PIGMENTOSA 56
RETINITIS PIGMENTOSA 56
0.600 CausalMutation CLINVAR

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C4015343
Disease: MACULAR DYSTROPHY, VITELLIFORM, 5
MACULAR DYSTROPHY, VITELLIFORM, 5
0.600 GeneticVariation CLINVAR

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C4015343
Disease: MACULAR DYSTROPHY, VITELLIFORM, 5
MACULAR DYSTROPHY, VITELLIFORM, 5
0.600 CausalMutation CLINVAR

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.420 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.420 GeneticVariation CLINVAR

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
0.420 CausalMutation CLINVAR

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0242383
Disease: Age related macular degeneration
Age related macular degeneration
0.110 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0730292
Disease: Macular dystrophy
Macular dystrophy
0.100 GeneticVariation CLINVAR Molecular genetic analysis using targeted NGS analysis of 677 individuals with retinal dystrophy. 30718709

2019

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.100 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.100 GeneticVariation GWASCAT Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease. 28067908

2017

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
0.100 CausalMutation CLINVAR Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa. 20673862

2010

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C4316870
Disease: Abnormality of the eye
Abnormality of the eye
0.100 CausalMutation CLINVAR Mutations in IMPG2, encoding interphotoreceptor matrix proteoglycan 2, cause autosomal-recessive retinitis pigmentosa. 20673862

2010

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0008525
Disease: Choroideremia
Choroideremia
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0009398
Disease: Color vision defect
Color vision defect
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
Diabetes Mellitus, Non-Insulin-Dependent
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0017601
Disease: Glaucoma
Glaucoma
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
Sensorineural Hearing Loss (disorder)
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0020459
Disease: Hyperinsulinism
Hyperinsulinism
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0020619
Disease: Hypogonadism
Hypogonadism
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0022578
Disease: Keratoconus
Keratoconus
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0028738
Disease: Nystagmus
Nystagmus
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0028754
Disease: Obesity
Obesity
0.100 Biomarker HPO

Entrez Id: 50939
Gene Symbol: IMPG2
IMPG2
CUI: C0029089
Disease: Ophthalmoplegia
Ophthalmoplegia
0.100 Biomarker HPO