Annotation Detail
Information
- Associated Genes
- FOXG1
- Associated Variants
-
FOXG1 MUTATION
FOXG1 MUTATION - Associated Disease
- Dysmorphic features
- Source Database
- DisGeNET
- Description
- Nucleotide alterations of the coding region of FOXG1 have never caused dysmorphic features.
- Pubmed
- 24139857
- Section of the abstract supporting the evidence
- BACKGROUND
- Number of the section of the abstract supporting the evidence
- 1
- Number of the sentence supporting the evidence
- 2
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.000271441872080303
Drugs