CELSR1

cadherin EGF LAG seven-pass G-type receptor 1
OMIM: 604523, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green CELSR1 in Hydrops fetalis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.313

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Lymphatic malformation 9, MIM# 619319

Green CELSR1 in Lymphoedema_nonsyndromic


Level 2: Cardiovascular disorders
Version 0.39

Component of the following Super Panels:

  • Vascular Malformations SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Lymphatic malformation 9, MIM# 619319

    Green CELSR1 in Mendeliome


    Version 1.1902

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Lymphatic malformation 9, MIM# 619319

    Green CELSR1 in Fetal anomalies


    Version 1.255

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Lymphatic malformation 9, MIM# 619319