Hurler disease
Case#: Patient 44, 5 years old (age at report), female, Indian
DiseaseAssertion: MPS1-H
FamilyInfo: N/A
CasePresentingHPOs: Coarse facial features, hepatosplenomegaly, joint contractures, corneal clouding, recurrent infections, dysostosis multiplex (HP:0000280, HP:0001433, HP:0002828, HP:0007957, HP:0002719, HP:0000943)
CaseHPOFreeText: N/A
CaseNotHPOs: N/A
CaseNotHPOFreeText: N/A
CaseEnzymeAssay: 2.0% (Range of residual enzyme activity: 0.0%-4.8%)
CaseUrineGAGs: N/A
CaseERT: N/A
CaseBMT: N/A
Variant1: c.1874A>G (p.Tyr625Cys)
Variant1ClinVarID: 100723
Variant1CAID: CA267584
Variant2: c.1874A>G (p.Tyr625Cys)
Variant2ClinVarID: 100723
Variant2CAID: CA267584
AdditionalVariants: N/A
ParentalGenotype: N/A
PreviouslyPublished N/A