# Correction to “Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)”

PMC · DOI: 10.1155/humu/9836575 · 2025-10-28

## Full-text entities

- **Genes:** PGAP2 (post-GPI attachment to proteins 2) [NCBI Gene 27315] {aka CWH43-N, FRAG1, HPMRS3, MRT17, MRT21}
- **Diseases:** HPMRS3 (OMIM:614207), Macrocephaly and Digital (MESH:D058627)

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Source: https://tomesphere.com/paper/PMC12585856