Page 6 - II-Congresso Nazionale ITALF

AUTOSOMAL DOMINANT
Gene
Protein
OMIM gene
Conditions
FLT4
Fms-Related Tyrosine Kinase 4
OMIM *136352
Milroy Disease
FOXC2
Forkhead Box C2
OMIM *602402
Lymphedema-distichiasis syndrome
GATA2
GATA Binding Protein 2
OMIM *137295
Emberger syndrome
GJC2
Gap Junction Protein, Gamma-2
OMIM *608803
Lymphedema, hereditary, IC
HGF
Hepatocyte Growth Factor
OMIM *142409
To define
MET
MET Protooncogene
OMIM *603514
To define
SOX18
SRY-BOX 18
OMIM *601618
Hypotrichosis-lymphedema- telangiectasia syndrome
VEGFC
Vascular Endothelial Growth Factor C
OMIM *601528
Lymphedema, hereditary, ID
KIF11
Kinesin Family Member 11
OMIM *148760
Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation