Lymphatic malformation 14

Summary

Lymphatic malformation-14 (LMPHM14) is an autosomal dominant disorder characterized by primary lymphedema (Greene et al., 2023). For a general phenotypic description and discussion of genetic heterogeneity of lymphatic malformation, see LMPHM1 (153100). [from OMIM]

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

ERG
39 tests
Also known as: LMPHM14, erg-3, p55, ERG
Summary: ETS transcription factor ERG

Imported from Human Phenotype Ontology (HPO)

Show all Hide all

Abnormality of metabolism/homeostasis
- Lymphedema
  Lymphedema
  - MedGen UID: 6155
  - Concept ID: C0024236
  - Finding: Disease or Syndrome
  Abnormality of metabolism/homeostasis
  See: Feature record | Search on this feature

Reviews

Clinical resources

Molecular resources

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.