Peroxisomal disordersGene: GRHPR
Link to peroxisomal disorders unclear.
Created: 20 Jul 2020, 10:14 a.m. | Last Modified: 20 Jul 2020, 10:14 a.m.
Panel Version: 1.6
Associated with phenotype in OMIM, not in G2P. At least eight variants reported
Created: 23 Aug 2016, 10:37 a.m.
Promoted to V1 3rd October 2016
Phenotypes for GRHPR were set to Hyperoxaluria, primary, type II 260000
GRHPR was added to Peroxisomal disorderspanel. Sources: Radboud University Medical Center, Nijmegen,UKGTN
GRHPR was created by sleigh
GRHPR was added to Peroxisomal disorderspanel. Sources: Illumina TruGenome Clinical Sequencing Services