Search Ontology:
Human Disease
Stargardt disease 5
- Term ID
- DOID:0061240
- Synonyms
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- Definition
- A stargardt disease that is characterized by onset of macular dystrophy in the fifth decade of life, with mildly reduced visual acuity and normal amplitudes on electroretinography and has_material_basis_in homozygous mutation in the RDH8 gene on chromosome 19p13. https://pubmed.ncbi.nlm.nih.gov/37628710/
- References
- Ontology
- Human Disease ( DOID:0061240 )
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Genes Involved
Zebrafish Models