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QuickView for primary congenital lymphedema (phenotype)


Genetic Markers

Most Correlated Genes

Most Correlated SNPs

  1. No genes found
  1. No SNPs found
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Pathway Enrichment

Most Correlated Biogroups

  1. Vascular endothelial growth factor receptor 3 (VEGFR3)
  2. VEGF-C-activated receptor activity
  3. DING_LUNG_CANCER_MUTATED_RECURRENTLY
  4. Tyrosine-protein kinase, receptor class III, conserved site
  5. MYLLYKANGAS_AMPLIFICATION_HOT_SPOT_27
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Curated Studies

Most Correlated Studies

  1. Mouse Phenotypes - Lymphedema
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Literature

Most Relevant Literature

  1. Primary congenital lymphedema complicated by hydrops fetalis: a case report and review of the litera…
  2. Milroy's primary congenital lymphedema in a male infant and review of the literature.
  3. Hereditary palmoplantar keratoderma associated with primary (congenital) lymphedema.
  4. Prenatal diagnosis of Milroy's primary congenital lymphedema.
  5. Recessive primary congenital lymphoedema caused by a VEGFR3 mutation.
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Clinical Trials

Most Relevant Clinical Trials

  1. Acupuncture for Chronic Lymphedema
  2. Acupuncture for the Treatment of Chronic Lymphedema
  3. Histologic Analysis of the Lymphatic Vessels Used for Supermicrosurgical Lymphatico-venous Anastomos…
  4. Effectiveness of Stellate Ganglion Block in Breast Cancer Related Lymphedema
  5. Physiological Study to Assess Mechanism of Action of MOBIDERM® in Lower-limb Lymphedema Patients
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