F13A1

coagulation factor XIII A chain
OMIM: 134570, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green F13A1 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.43

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Factor XIIIA deficiency, MIM# 613225
  • MONDO:0013187

Green F13A1 in Mendeliome


Version 1.1902

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Factor XIIIA deficiency, MIM# 613225
  • MONDO:0013187

Green F13A1 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Factor XIIIA deficiency, MIM# 613225

Green F13A1 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.114

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • BeginNGS
  • Expert list
Phenotypes
  • Factor XIIIA deficiency, MIM# 613225
Tags
  • treatable
  • haematological

Green F13A1 in Transplant Co-Morbidity Superpanel


Level 2: Screening
Version 0.18

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Factor XIIIA deficiency, MIM# 613225
  • MONDO:0013187