VWA1

von Willebrand factor A domain containing 1
OMIM: 611901
PanelMode of inheritanceDetails
1 panel
R-numbers: R78
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Neuropathy, hereditary motor, with myopathic features OMIM:619216, neuropathy, hereditary motor, with myopathic features MONDO:0030977