APOA2

apolipoprotein A2
OMIM: 107670, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Green APOA2 in Periodic fever syndromes

Level 3: Multi-system inflammatory/autoimmune disorders
Level 2: Rheumatological disorders
Version 1.34

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Amyloidosis
Red APOA2 in Familial hypercholesterolaemia

Level 3: Arteriopathies
Level 2: Cardiovascular disorders
Version 1.31

review Not set
Sources
  • Radboud University Medical Center, Nijmegen
Phenotypes
  • Apolipoprotein A-II deficiency {Hypercholesterolemia, familial, modification of}, 143890
Green APOA2 in Hereditary systemic amyloidosis


Level 2: Renal
Version 1.28
Latest signed off version: v1.24 (30 Apr 2025)

Component of the following Super Panels:

  • Unexplained young onset end-stage renal disease
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • NHS GMS
    • Expert Review Green