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Sveinsson chorioretinal atrophy; atrophia areata; helicoidal peripapillary chorioretinal degeneration
Pathology:
- symmetrical lesions radiating from the optic disk involving the retina & the choroid
Genetics:
- autosomal_dominant
- associated with defects in TEAD1
Clinical manifestations:
- myopia
- astigmatism
General
genetic disease of the eye
retinal disease
Database Correlations
OMIM 108985
References
UniProt :accession P28347