Disease: Chorioretinal Atrophy, Progressive Bifocal

Name Chorioretinal Atrophy, Progressive Bifocal


Classification eye, genetic

Phenotypes Autosomal dominant inheritance; Chorioretinal atrophy; Chorioretinal dystrophy; Myopia; Nystagmus; Retinal detachment; Visual impairment

Associated Genes -

Mouse Orthologs -

Source OMIM:600790 (names, synonyms, disease associated genes),
Orphanet (disease classes),
HGNC, Ensembl, MGI (gene symbols, gene orthology)
HPO (phenotypes)

Mouse Model: phenotype-based associations

Disease phenotypes are compared with mouse phenotypes, with each mouse model contributing one point to the diagram. Scores are computed according to phenotype specificity and cross-species similarity. X-axis shows the score of the single phenotype that contributes most. Y-axis shows an average among all phenotype matches. The curved line designates a visualization threshold; models below threshold are omitted, except when their genotype matches a disease-associated gene.

Mouse Models

No mouse models associated with OMIM:600790 by orthology to a human gene.

The IMPC Newsletter

Get highlights of the most important data releases, news and events, delivered straight to your email inbox

Subscribe to newsletter