Human genes for central conducting lymphatic anomaly
Central conducting lymphatic anomaly [DOID:0081030]
A lymphatic system disease that is characterized by dysfunction of the thoracic duct or cisterna chyli, leading to a retrograde flux of lymphatic fluid or abnormal drainage of lymphatic fluid and that has_material_basis_in heterozygous mutation in the EPHB4 gene on chromosome 7q22.
Synonyms: central conducting lymphatic anomaly, central conducting lymphatic anomalies, DOID:0081030, lymphatic malformation-7, lymphatic malformation7