ENO1

enolase 1
OMIM: 172430, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red ENO1 in Polymicrogyria and Schizencephaly


Level 2: Neurology and neurodevelopmental disorders
Version 0.195

Component of the following Super Panels:

  • Malformations of cortical development_Superpanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Polymicrogyria, MONDO:0000087, ENO1-related

    Red ENO1 in Mendeliome


    Version 1.2374

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Polymicrogyria, MONDO:0000087, ENO1-related

    Red ENO1 in Fetal anomalies


    Version 1.314

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Expert list
    Phenotypes
    • Polymicrogyria, MONDO:0000087, ENO1-related