Retinoschisis, Autosomal Dominant - CISMeF

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CISMeF

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Retinoschisis, Autosomal DominantMeSH concept

Preferred Label : Retinoschisis, Autosomal Dominant;

Details

Origin ID

M000606800;

CISMeF manual mappings
- Retinoschisis, autosomal dominant [OMIM Phenotype]
Related record
- Retinoschisis, Autosomal Dominant [MeSH Supplementary Concept]

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27/05/2025

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