Version: 8.0.0
Date: Tue Jan 28 2025
Leber congenital amaurosis 9
DOID:0110005
SummaryAssociated GenesAssociated AllelesAssociated Models
Disease

Leber congenital amaurosis 9

Definition
A Leber congenital amaurosis that has_material_basis_in mutation in the NMNAT1 gene on chromosome 1p36.
Synonyms
  • LCA9
Cross References
Parent Terms
Child Terms
None
Sources of Associations

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      Associated Models

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