# Syndromology at the interface of evolving phenotypes, epimutations, and model systems

**Authors:** Nuria C. Bramswig, Dagmar Wieczorek

PMC · DOI: 10.1515/medgen-2024-2024 · 2024-06-06

## Full-text entities

- **Diseases:** multiple disabilities (MESH:D003147), rare (MESH:D035583), genetic diseases (MESH:D030342), syndromic diseases (MESH:D004194), developmental and psychiatric disorders (MESH:D001523), Costello syndrome (MESH:D056685)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11154180/full.md

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Source: https://tomesphere.com/paper/PMC11154180