Lymphatic malformation 3

MONDO:0013278

Any hereditary lymphedema in which the cause of the disease is a mutation in the GJC2 gene.

Also known as: GJC2 hereditary lymphedema, hereditary lymphedema caused by mutation in GJC2, lymphedema, hereditary, 1C, lymphedema, hereditary, type 1C, LMPH1C, lymphedema, hereditary, IC

1 clinical trial for this condition and its sub-types, 0 tagged with Lymphatic malformation 3 itself.

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Including sub-types (1) Tagged with Lymphatic malformation 3 (0)

Trials to join now! 1

Massive study launches to unravel mysteries of rare lymphatic diseases

Knowledge-focused Recruiting now

This natural history study aims to collect data from 1,200 people with lymphatic anomalies—rare conditions affecting the body's lymph system—over many years. Researchers will track symptoms, perform genetic testing, and gather biospecimens to better understand why these condition…

Sponsor: Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) • Aim: Knowledge-focused

Last updated Aug 08, 2026 00:03 UTC

Lymphatic malformation 3

Where it sits in the disease tree

Massive study launches to unravel mysteries of rare lymphatic diseases