FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term central conducting lymphatic anomaly ID (Ontology) DOID:0081030 (Human Disease)
Definition 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.
Also Known As "lymphatic malformation-7"
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 Genes
 central conducting lymphatic anomaly       1
 for disease ribbon | central conducting lymphatic anomaly       1
 model of | central conducting lymphatic anomaly       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
immune system disease           |
 |__lymphatic system disease____|
                                central conducting lymphatic anomaly  1 rec.
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Is a autosomal dominant disease
lymphatic system disease
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Synonyms
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MIM:617300