FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term lymphedema-distichiasis syndrome ID (Ontology) DOID:0111509 (Human Disease)
Definition A syndrome characterized by lymphedema of the limbs and double rows of eyelashes that has_material_basis_in heterozygous mutation in the FOXC2 gene on chromosome 16q24.1.
Also Known As "LPHDST" ; "lymphedema with distichiasis"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 lymphedema-distichiasis syndrome       1
 for disease ribbon | lymphedema-distichiasis syndrome       1
 model of | lymphedema-distichiasis syndrome       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
                                lymphedema-distichiasis syndrome  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "LPHDST" EXACT OMO:0003012
    "lymphedema with distichiasis" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
GARD:333
MESH:C537710
MIM:153400
NCI:C128191
ORDO:33001
SNOMEDCT_US_2023_03_01:8634009
UMLS_CUI:C0265345