FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term multiple cutaneous and mucosal venous malformations ID (Ontology) DOID:0050792 (Human Disease)
Definition A vein disease that is characterized by multiple bluish cutaneous or mucosal venous lesions that has_material_basis_in heterozygous mutation in the TEK gene on chromosome 9p21.
Also Known As "cutaneomucosal venous malformation" ; "mucocutaneous venous malformations" ; "VMCM"
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
 multiple cutaneous and mucosal venous malformations       3
 for disease ribbon | multiple cutaneous and mucosal venous malformations       3
 model of | multiple cutaneous and mucosal venous malformations       3
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal dominant disease__
integumentary system disease    |
 |__skin disease________________|
vascular disease                |
 |__vein disease________________|
                                multiple cutaneous and mucosal venous malformations  3 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal dominant disease
skin disease
vein disease
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "cutaneomucosal venous malformation" EXACT
    "mucocutaneous venous malformations" EXACT
    "VMCM" EXACT OMO:0003012
Secondary IDs
hide External Crossreferences & Linkouts
MESH:C563977
MIM:600195
ORDO:2451
SNOMEDCT_US_2023_03_01:699301008
UMLS_CUI:C1838437