Version: 8.0.0
Date: Tue Jan 28 2025
Leber congenital amaurosis 7
DOID:0110333
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

Leber congenital amaurosis 7

Definition
A Leber congenital amaurosis that has_material_basis_in mutation in the CRX gene on chromosome 19q13.
Synonyms
  • LCA7
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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