Annotation Detail
Information
- Associated Genes
- FOXG1
- Associated Variants
-
FOXG1 MUTATION
FOXG1 MUTATION - Associated Disease
- FOXG1 syndrome
- Source Database
- DisGeNET
- Description
- A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndrome.
- Pubmed
- 24139857
- Section of the abstract supporting the evidence
- TITLE
- Number of the section of the abstract supporting the evidence
- 0
- Number of the sentence supporting the evidence
- 0
- Original source reporting the Gene Disease association
- BeFree,CLINVAR,CTD_human,UNIPROT
- DisGENET score for the Gene Disease association
- 0.364343069953285
Drugs