ANGPT2

PanelMode of inheritanceDetails
1 panel
R-numbers: R21, R412
Signed-off version 5.0
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Phenotypes
hydrops fetalis, MONDO:0015193, Lymphatic malformation 10, OMIM:619369, lymphatic malformation 10, MONDO:0023662