VEGFC

vascular endothelial growth factor C
OMIM: 601528
PanelMode of inheritanceDetails
2 panels
R-numbers: R21, R412
Signed-off version 2.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Lymphatic malformation 4
R-numbers: R136
Signed-off version 3.1
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Lymphedema, hereditary, ID 615907 (Primary Lymphoedema, Milroy-like)