Lymphedema–distichiasis syndrome is a medical condition associated with the FOXC2 gene.: 849  People with this hereditary condition have a double row of...

syndrome, lymphedema–distichiasis syndrome, yellow nail syndrome, and Klippel–Trénaunay syndrome. One defined genetic cause for hereditary lymphedema...

of a study published in 1968, were alive at the time. Lymphedema-distichiasis syndrome Lymphedema praecox Blueberry muffin baby Rapini, Ronald P.; Bolognia...

form of primary lymphedema, accounting for about 80% of the patients.: 848  Lymphedema Lymphedema-distichiasis syndrome Aagenaes syndrome List of cutaneous...

syndrome Lujan–Fryns syndrome Lutembacher's syndrome Lymphangitis carcinomatosa Lymphedema–distichiasis syndrome Lynch syndrome Lyngstadaas syndrome Löffler's...

Pitt–Hopkins syndrome (PTHS) is a rare genetic disorder characterized by developmental delay, epilepsy, distinctive facial features, and possible intermittent...

the lower extremities Lymphedema–distichiasis syndrome, a genetic disorder of eyelashes and lymphatic system Loeys–Dietz syndrome, a genetic disorder affecting...

neoplasm Lymphedema distichiasis Lymphedema hereditary type 1 Lymphedema hereditary type 2 Lymphedema ptosis Lymphedema, congenital Lymphedema Lymphedema–distichiasis...

FOXC1 Axenfeld syndrome 3 Iridogoniodysgenesis, dominant type FOXC2 Lymphedema–distichiasis syndrome FOXE1 Bamforth–Lazarus syndrome FOXE3 Anterior segment...

syndrome, segmental hyalinizing vasculitis) Lymphedema praecox Lymphedema–distichiasis syndrome Maffucci syndrome Majocchi's disease (purpura annularis telangiectodes...