Search Ontology:
Human Disease

Stargardt disease 4

Term ID
DOID:0061239
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. https://pubmed.ncbi.nlm.nih.gov/15557430/
References
Ontology
Human Disease   ( DOID:0061239 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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