KLKB1

kallikrein B1
OMIM: 229000, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber KLKB1 in Bleeding and Platelet Disorders


Level 2: Haematological disorders
Version 1.43

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert Review
Phenotypes
  • Fletcher factor (prekallikrein) deficiency, MIM# 612423

Amber KLKB1 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Fletcher factor (prekallikrein) deficiency, MIM# 612423