1. Genes and Genomic Entities
  2. NXN

NXN

nucleoredoxin
OMIM: 612895, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Amber NXN in Limb disorders


Version 4.18
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert list
    Phenotypes
    • Robinow syndrome, autosomal recessive 2, 618529
    Tags
    • watchlist
    Green NXN in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 4.56
    Latest signed off version: v4.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    • Literature
    Phenotypes
    • Robinow syndrome, autosomal recessive 2, OMIM:618529
    Green NXN in Fetal anomalies


    Version 3.155
    Latest signed off version: v3.0 (22 Mar 2023)

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Robinow syndrome, autosomal recessive 2, OMIM:618529
    • Robinow syndrome, autosomal recessive 2, MONDO:0032800