VWA3B

von Willebrand factor A domain containing 3B
OMIM: 614884, ClinGen, DECIPHER

1 panel

Panel Reviews Mode of inheritance Details
1 panel

Red VWA3B in Ataxia - adult onset


Level 2: Neurology and neurodevelopmental disorders
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • GeneReviews
  • Royal Melbourne Hospital
  • Expert Review Red
Phenotypes
  • ?Spinocerebellar ataxia, autosomal recessive 22