congenital disorder of glycosylation, type IIaa
MONDO:0957540Mondo
Findings
No curated finding names congenital disorder of glycosylation, type IIaa 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
24 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.
- CholestasisHPOHP:0001396
- 2 of 2 reported patients
- Elevated circulating alkaline phosphatase concentrationHPOHP:0003155
- 2 of 2 reported patients
- Elevated circulating aspartate aminotransferase concentrationHPOHP:0031956
- 2 of 2 reported patients
- Hepatic failureHPOHP:0001399
- 2 of 2 reported patients
- HepatomegalyHPOHP:0002240
- 2 of 2 reported patients
- HyperammonemiaHPOHP:0001987
- 2 of 2 reported patients
- HypercholesterolemiaHPOHP:0003124
- 2 of 2 reported patients
- HypoglycemiaHPOHP:0001943
- 2 of 2 reported patients
- HypotoniaHPOHP:0001252
- 2 of 2 reported patients
- Narrow chestHPOHP:0000774
- 2 of 2 reported patients
- Reduced antithrombin III activityHPOHP:0001976
- 2 of 2 reported patients
- Reduced protein C activityHPOHP:0005543
- 2 of 2 reported patients
Show the remaining 12
- Short long boneHPOHP:0003026
- 2 of 2 reported patients
- Bilateral talipes equinovarusHPOHP:0001776
- 1 of 2 reported patients
- Biliary cirrhosisHPOHP:0002613
- 1 of 2 reported patients
- Hepatic fibrosisHPOHP:0001395
- 1 of 2 reported patients
- HydronephrosisHPOHP:0000126
- 1 of 2 reported patients
- Knee flexion contractureHPOHP:0006380
- 1 of 2 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.
- STX5HGNC:11440
- Limited · Ambry Genetics · Autosomal recessive · 2023