factor XIII, A subunit, deficiency of
MONDO:0013187Mondo
Findings
No curated finding names factor XIII, A 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
- Onset and course
- Neonatal onset
HPO, annotations 2026-09-02
Features
9 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
- 2 of 2 reported patients
- Abnormal umbilical stump bleedingHPOHP:0011884
- 2 of 2 reported patients
- Bruising susceptibilityHPOHP:0000978
- 2 of 2 reported patients
- EcchymosisHPOHP:0031364
- 2 of 2 reported patients
- Factor XIII subunit A deficiencyHPOHP:0040233
- 2 of 2 reported patients
- Gingival bleedingHPOHP:0000225
- 2 of 2 reported patients
- Reduced factor XIII activityHPOHP:0008357
- 2 of 2 reported patients
- Persistent bleeding after traumaHPOHP:0001934
- 1 of 2 reported patients
- Spontaneous hematomasHPOHP:0007420
- 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.
- F13A1HGNC:3531
- Definitive · ClinGen · Autosomal recessive · 2020
- Definitive · Laboratory for Molecular Medicine · Autosomal recessive · 2020
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal recessive · 2022
- Strong · PanelApp Australia · Autosomal recessive · 2025
Where it sits
Other names
4 names
Resolves to: factor XIII, A subunit, deficiency of
- Also called
- factor XIIIA deficiencyhereditary factor XIII A subunit deficiencyhereditary factor XIII alpha subunit deficiencyhereditary factor XIII type II deficiency