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 0.427

Component of the following Super Panels:

  • Neuromuscular Superpanel
  • 1 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 1.3512

    1 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

    0 reviews Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green PRG4 in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.110

    0 reviews 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 1.465

    1 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 2.14

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