FG syndrome 3
MONDO:0010316Mondo
Findings
No curated finding names FG syndrome 3 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- X-linked inheritance
- Onset and course
- Death in infancy · Congenital onset
HPO, annotations 2026-09-02
Features
18 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.
- Broad halluxHPOHP:0010055
- 4 of 4 reported patients
- Broad thumbHPOHP:0011304
- 4 of 4 reported patients
- Chronic constipationHPOHP:0012450
- 3 of 3 reported patients
- Fine hairHPOHP:0002213
- 2 of 2 reported patients
- Frontal upsweep of hairHPOHP:0002236
- 3 of 3 reported patients
- HyperactivityHPOHP:0000752
- 3 of 3 reported patients
- HypotoniaHPOHP:0001252
- 5 of 5 reported patients · Neonatal onset
- Intellectual disabilityHPOHP:0001249
- 6 of 6 reported patients
- Prominent foreheadHPOHP:0011220
- 5 of 5 reported patients
- Relative macrocephalyHPOHP:0004482
- 4 of 4 reported patients
- Sparse hairHPOHP:0008070
- 2 of 2 reported patients
- Feeding difficultiesHPOHP:0011968
- 3 of 4 reported patients
Show the remaining 6
- Joint contractureHPOHP:0034392
- 2 of 3 reported patients
- CryptorchidismHPOHP:0000028
- 1 of 4 reported patients
- Agenesis of corpus callosumHPOHP:0001274
- 1 of 6 reported patients
- Chiari type I malformationHPOHP:0007099
- 1 of 6 reported patients
- Pyloric stenosisHPOHP:0002021
- 0 of 3 reported patients
- Sensorineural hearing impairmentHPOHP:0000407
- 0 of 3 reported patients
Where it sits
- A kind of