Term Name: Leber congenital amaurosis 15
Synonyms: LCA15
Definition: A Leber congenital amaurosis that has_material_basis_in mutation in the TULP1 gene on chromosome 6p21.3.
Ontology: Human Disease [DOID:0110189]   ( DOID:0110189 )

Relationships
is a type of: autosomal recessive disease Leber congenital amaurosis