congenital disorder of glycosylation with defective fucosylation 1
MONDO:0020775Mondo
Findings
No curated finding names congenital disorder of glycosylation with defective fucosylation 1 yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive inheritance
- Onset and course
- Congenital onset
HPO, annotations 2026-09-02
Features
32 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.
- Failure to thriveHPOHP:0001508
- 3 of 3 reported patients
- Feeding difficultiesHPOHP:0011968
- 3 of 3 reported patients
- HypotoniaHPOHP:0001252
- 3 of 3 reported patients
- Intellectual disabilityHPOHP:0001249
- 3 of 3 reported patients
- Intrauterine growth retardationHPOHP:0001511
- 3 of 3 reported patients
- Limb undergrowthHPOHP:0009826
- 3 of 3 reported patients
- MicrocephalyHPOHP:0000252
- 3 of 3 reported patients
- SeizureHPOHP:0001250
- 3 of 3 reported patients
- Severe global developmental delayHPOHP:0011344
- 3 of 3 reported patients
- Short statureHPOHP:0004322
- 3 of 3 reported patients
- PolyhydramniosHPOHP:0001561
- 2 of 3 reported patients
- Atrial septal defectHPOHP:0001631
- 1 of 3 reported patients
Show the remaining 20
- Broad foreheadHPOHP:0000337
- 1 of 3 reported patients
- BuphthalmosHPOHP:0000557
- 1 of 3 reported patients
- Decreased total neutrophil countHPOHP:0001875
- 1 of 3 reported patients
- GlaucomaHPOHP:0000501
- 1 of 3 reported patients
- High foreheadHPOHP:0000348
- 1 of 3 reported patients
- High palateHPOHP:0000218
- 1 of 3 reported patients
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- FUT8HGNC:4019
- Definitive · ClinGen · Autosomal recessive · 2024
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2020
- Strong · G2P · Autosomal recessive · 2025
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2020