VWA8

von Willebrand factor A domain containing 8
OMIM: 617509, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green VWA8 in Retinitis pigmentosa


Level 2: Ophthalmological disorders
Version 1.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Expert Review Green
  • Expert Review Green
  • Literature
Phenotypes
  • Retinitis pigmentosa 97, MIM#620422

Green VWA8 in Retinitis pigmentosa_Autosomal Dominant


Level 2: Ophthalmological disorders
Version 1.0

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Retinitis pigmentosa 97, MIM#620422