F10

coagulation factor X
OMIM: 613872, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green F10 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 X deficiency, MIM# 227600
  • MONDO:0009212

Green F10 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Factor X deficiency, MIM# 227600
  • MONDO:0009212

Green F10 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Factor X deficiency, MIM# 227600

Green F10 in BabyScreen+ newborn screening


Level 2: Screening
Version 1.113

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert list
Phenotypes
  • Factor X deficiency, MIM# 227600
Tags
  • treatable
  • haematological

Green F10 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 X deficiency, MIM# 227600
  • MONDO:0009212