Any hereditary lymphedema in which the cause of the disease is a mutation in the VEGFC gene.
Comprehensive, easy-to-understand information about this condition
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microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
MONDO:0007918
lymphatic malformation 1
MONDO:0007919
lymphatic malformation 5
MONDO:0007920
yellow nail syndrome
MONDO:0007921
lymphedema-distichiasis syndrome
MONDO:0007922
campomelia, Cumming type
MONDO:0008896