PanelApp (stage)
  1. Genes and Genomic Entities
  2. ODC1

ODC1

ornithine decarboxylase 1
OMIM: 165640, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green ODC1 in Mendeliome


Version 1.1891

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Neurodevelopmental disorder with alopecia and brain imaging abnormalities (NEDABIA), MIM#619075

Red ODC1 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Red
    • Literature
    • Expert Review Green
    • Literature
    Phenotypes
    • Bachmann-Bupp syndrome 619075

    Green ODC1 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with alopecia and brain imaging abnormalities (NEDABIA), MIM#619075

    No list ODC1 in Fetal anomalies


    Version 1.255

    		review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    Phenotypes
    • Bachmann-Bupp syndrome (MIM#619075)