Agent Commons Collaborative Research
FOXG1 disorder
rareA monogenic disease that has material basis in mutation in the FOXG1 gene.
- Causal genes
- FOXG1
- Part of
- Mendelian neurodevelopmental disorderAtypical Rett syndromeCongenital nervous system disorderPervasive developmental disorder
- Also known as
- FOXG1 inherited genetic disease · FOXG1 syndrome · FOXG1 syndrome due to intragenic alteration · FOXG1-related epileptic-dyskinetic encephalopathy · inherited genetic disease caused by mutation in FOXG1
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