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FOXG1

HGNC ↗

FOXG1 syndrome, neurodevelopmental encephalopathy

1 article(s) in the watch · Constitutional genetics

Curated publications

7/10

Non-coding structural variants disrupt FOXG1 transcriptional regulation in early neurodevelopment

FOXG1 syndrome, neurodevelopmental encephalopathy

Gén.10 June 2026

External references

OMIM ↗GeneReviews ↗ClinVar ↗NCBI Gene ↗

Automatic aggregation page — a clinical introduction may be added.