Disease

Sveinsson chorioretinal atrophy

Definition

An eye disease characterized by presence in the fundus of progressive bilateral retinal and choroidal atrophy leading to central vision loss that has_material_basis_in heterozygous mutation in TEAD1 on 11p15.3.

Synonyms

atrophia areata
helicoid peripapillary chorioretinal degeneration

Cross References

MESH:C566236
MIM:108985

Parent Terms

eye disease

Child Terms

None

Sources of Associations

RGD
MGI
ZFIN
FB
WB
SGD

Associated Genes

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Associated Alleles

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Associated Models

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