factor XIII, b subunit, deficiency of
MONDO:0013190Mondo
Findings
No curated finding names factor XIII, b subunit, deficiency of yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal recessive 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.
- Abnormal bleedingHPOHP:0001892
- 1 of 1 reported patient
- Factor XIII subunit B deficiencyHPOHP:0040234
- 2 of 2 reported patients
- Reduced factor XIII activityHPOHP:0008357
- 3 of 3 reported patients
- Abnormal umbilical stump bleedingHPOHP:0011884
- 1 of 2 reported patients · Neonatal onset
- Prolonged bleeding after surgeryHPOHP:0004846
- 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.
- F13BHGNC:3534
- Definitive · ClinGen · Autosomal recessive · 2020
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2018
- Strong · PanelApp Australia · Autosomal recessive · 2025
- Moderate · Ambry Genetics · Autosomal recessive · 2023
Where it sits
Other names
1 name
Resolves to: factor XIII, b subunit, deficiency of
- Also called
- factor XIIIB deficiency