The NM_000203.5:c. c.123G>A (p.Trp41Ter) variant in IDUA is a nonsense variant predicted to cause a premature stop codon in biologically-relevant-exon 1 out of 14, leading to nonsense mediated decay in a gene in which loss-of-function is an established disease mechanism (PVS1). This variant has been detected in at least one individual with Hurler syndrome, presenting with IDUA deficiency within the affected range, increased excretion of urinary dermatan sulfate and heparan sulfate, and clinical features specific to MPS I including Macrocephaly, joint stiffness, Mongolian macula, hepatosplenomegaly, hernia, cardiac disease, and airway obstruction (PMID 21480867) (PP4_moderate). This individual is compound heterozygous for the variant and c.300-1G>C, p.(?). The allelic data for this patient will be used to support the classification of c.300-1G>C and is not included here in order to avoid circular logic. The highest population minor allele frequency in gnomAD v4.1.0 is 8.889e-7 (1/1,124,963 alleles) in the Non-Finnish European population, which is lower than the ClinGen Lysosomal Diseases VCEP’s threshold for PM2_Supporting (>0.00025), meeting this criterion (PM2_Supporting). There is a ClinVar entry for this variant (Variation ID: 2734632). In summary, this variant meets the criteria to be classified as pathogenic for MPS I based on the IDUA-specific ACMG/AMP criteria applied, as specified by the ClinGen Lysosomal Diseases Variant Curation Expert panel (Specifications Version 1.0.0): (PVS1, PP4 moderate, PM2 supporting). (Classification approved by the ClinGen Lysosomal Diseases Variant Curation Expert Panel on April 7, 2025)