FG syndrome 2
MONDO:0010297Mondo
Findings
No curated finding names FG syndrome 2 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any FG syndrome in which the cause of the disease is a mutation in the FLNA gene.
Definition from the Mondo Disease Ontology (MONDO:0010297), read 2026-09-29. CC BY 4.0.
- Inheritance
- X-linked inheritance
HPO, annotations 2026-09-02
Features
5 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- ConstipationHPOHP:0002019
- Delayed speech and language developmentHPOHP:0000750
- Large foreheadHPOHP:0002003
- Neonatal hypotoniaHPOHP:0001319
- Underdeveloped superior crus of antihelixHPOHP:0011246
Where it sits
- A kind of
Other names
3 names
Resolves to: FG syndrome 2
- Also called
- FG syndrome caused by mutation in FLNAFG syndrome type 2FLNA FG syndrome