PanelApp (stage)
  1. Genes and Genomic Entities
  2. FCN3

FCN3

ficolin 3
OMIM: 604973, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber FCN3 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Victorian Clinical Genetics Services
Phenotypes
  • Immunodeficiency due to ficolin 3 deficiency, MIM# 613860

Amber FCN3 in Complement Deficiencies


Level 2: Immunological disorders
Version 0.73

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Immunodeficiency due to ficolin 3 deficiency, MIM# 613860