Version: 8.0.0
Date: Tue Jan 28 2025
Leber congenital amaurosis 13
DOID:0110330
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

Leber congenital amaurosis 13

Definition
A Leber congenital amaurosis thatis characterized by mild or absent hyperopia, transient improvement of visual acuity, and eventual macular atrophy with severe disease progression and has_material_basis_in mutation in the RDH12 gene on chromosome 14q23.3.
Synonyms
  • LCA13
Cross References
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None
Sources of Associations

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