PRG4

proteoglycan 4
OMIM: 604283, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green PRG4 in Arthrogryposis


Level 2: Neurology and neurodevelopmental disorders
Version 0.411

Component of the following Super Panels:

  • Neuromuscular Superpanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, MIM# 208250

    Green PRG4 in Mendeliome


    Version 1.1891

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, MIM# 208250

    Green PRG4 in Short Long Bones with Advanced Carpal Bone Age


    Level 2: Skeletal disorders
    Version 0.1

    review Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green PRG4 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.109

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, 208250 (3)

    Green PRG4 in Fetal anomalies


    Version 1.255

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Camptodactyly-arthropathy-coxa vara-pericarditis syndrome 208250

    Green PRG4 in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, 208250 (3)