VTN:Ensemblv115

vitronectin
OMIM: 193190, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red VTN in Atypical Haemolytic Uraemic Syndrome_MPGN


Level 2: Renal and urinary tract disorders
Version 1.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Red
Phenotypes
  • Atypical haemolytic uraemic syndrome