Multiple cutaneous and mucosal venous malformations

Summary

The condition multiple cutaneous and mucosal venous malformations (VMCM) is characterized by the presence of small, multifocal bluish cutaneous and/or mucosal venous malformations. They are usually present at birth. New lesions appear with time. Small lesions are usually asymptomatic; larger lesions can invade subcutaneous muscle and cause pain. Malignant transformation has not been reported. [from GeneReviews]

Available tests

36 tests are in the database for this condition.

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Clinical tests (35 available)

Molecular Genetics Tests

Research tests

See all research tests for this condition (1)

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

TEK
57 tests
Also known as: CD202B, GLC3E, TIE-2, TIE2, VMCM, VMCM1, TEK
Summary: TEK receptor tyrosine kinase

Imported from Human Phenotype Ontology (HPO)

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Abnormality of the cardiovascular system
- Venous malformation
  Venous malformation
  - MedGen UID: 754284
  - Concept ID: C2937220
  - Finding: Congenital Abnormality
  Abnormality of the cardiovascular system
  See: Feature record | Search on this feature
Abnormality of the digestive system
- Intestinal bleeding
  Intestinal bleeding
  - MedGen UID: 75632
  - Concept ID: C0267373
  - Finding: Finding
  Abnormality of the digestive system
  See: Feature record | Search on this feature

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