Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
An inherited retinopathy caused by bi-allelic variants in the MERTK gene.
No clinical trials have been registered for MERTK-related retinopathy.
5 publications have been identified in PubMed for MERTK-related retinopathy. Research spans Basic Science / Preclinical (80%) and Epidemiology / Natural History (20%).
Khan AO (2026). [PMID: 41166683](https://pubmed.ncbi.nlm.nih.gov/41166683/). *Retina*. [Epidemiology / Natural History]
Liu P (2025). [PMID: 40374315](https://pubmed.ncbi.nlm.nih.gov/40374315/). *Aging Cell*. [Basic Science / Preclinical]
Yilmaz C (2025). [PMID: 40456730](https://pubmed.ncbi.nlm.nih.gov/40456730/). *Cell Death Dis*. [Basic Science / Preclinical]
Hesaraki M (2025). [PMID: 41030050](https://pubmed.ncbi.nlm.nih.gov/41030050/). *Cell J*. [Basic Science / Preclinical]
Bu S (2024). [PMID: 39845889](https://pubmed.ncbi.nlm.nih.gov/39845889/). *Front Endocrinol (Lausanne)*. [Basic Science / Preclinical]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 11:22 AM UTC
Common questions about MERTK-related retinopathy