VPS33A

VPS33A, CORVET/HOPS core subunit
OMIM: 610034, ClinGen, DECIPHER

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green VPS33A in Mendeliome


Version 1.4230

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Mucopolysaccharidosis-plus syndrome (MIM#617303)

Green VPS33A in Lysosomal Storage Disorder


Level 2: Metabolic conditions
Version 1.27

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Mucopolysaccharidosis-plus syndrome (MIM#617303)

    Green VPS33A in Skeletal dysplasia

    Level 3: Skeletal dysplasias
    Level 2: Skeletal disorders
    Version 0.402

    2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Victorian Clinical Genetics Services
    Phenotypes
    • Mucopolysaccharidosis-plus syndrome (MIM#617303)