VPS33A

VPS33A, CORVET/HOPS core subunit
OMIM: 610034
PanelMode of inheritanceDetails
2 panels
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R98
Signed-off version 5.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mucopolysaccharidosis-plus syndrome OMIM:617303, mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders MONDO:0015012
R-numbers: R276
Signed-off version 3.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Mucopolysaccharidosis-plus syndrome OMIM:617303, mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders MONDO:0015012