| Metadata | |
|---|---|
| ID | DOID:0061239 |
| PURL | http://purl.obolibrary.org/obo/DOID_0061239 Copy |
| Name | Stargardt disease 4 |
| 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. https://pubmed.ncbi.nlm.nih.gov/15557430/ |
| Xrefs | |
| Parent Relationships |
is_a Stargardt disease |
| Subclass Logical Relationships |
has material basis in some autosomal dominant inheritance |