Term Name:
Leber congenital amaurosis 12
Synonyms:
LCA12
Definition:
A Leber congenital amaurosis that has_material_basis_in mutation in the RD3 gene on chromosome 1q32.
Ontology:
Human Disease [DOID:0110080] (
DOID:0110080
)
Relationships
is a type of:
autosomal recessive disease
Leber congenital amaurosis