Search Ontology:
Human Disease

Stargardt disease 3

Term ID
DOID:0061238
Synonyms
Definition
A stargardt disease that is characterized by macular pigmentary changes and yellow flecks and macular retinal pigment epithelium defects and has_material_basis_in heterozygous mutation in the ELOVL4 gene on chromosome 6q14. https://pubmed.ncbi.nlm.nih.gov/15557430/
References
Ontology
Human Disease   ( DOID:0061238 )
Relationships
Other Pages
Genes Involved
Zebrafish Models
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