Term Name: Stargardt disease 4
Synonyms:
Definition: A stargardt disease that is characterized by decreased central vision, atrophy of the macula and underlying retinal pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina and has_material_basis_in heterozygous mutation in the prominin-1 gene on chromosome 4p15.
Ontology: Human Disease [DOID:0061239]   ( DOID:0061239 )

Relationships
is a type of: Stargardt disease