mucopolysaccharidosis type 1 https://www.malacards.org/card/scheie_syndrome mucopolysaccharidosis type I Hurler syndrome (subtype) GARD:0010335 MPSI SCTID:75610003 Mucopolysaccharidosis Type I Scheie syndrome (subtype) formerly known as Mucopoly-saccharidosis type V) MONDO:0001586 The most common type of mucopolysaccharidosis. It is inherited in an autosomal recessive pattern. It comprises a group of lysosomal storage diseases which includes the most severe form (Hurler syndrome) and the mildest form (Scheie syndrome). NCIT:C85053 Orphanet:579 attenuated MPS I (subtype, includes Hurler-Scheie and Scheie syndrome) MedDRA:10056886 NORD:1462 Hurler-Scheie syndrome (subtype) NANDO:2200547 DOID:12802 mucopolysaccharidosis type 1 lipochondrodystrophy severe MPS I (subtype, also known as Hurler syndrome) Alpha-L-iduronidase deficiency MPS 1 NANDO:2201168 IDUA deficiency MEDGEN:44171 UMLS:C0023786 MPS1 icd11.foundation:1539226250 MPS I Hurler syndrome eye disorder bone disorder mucopolysaccharidosis obsolete eyebrow hypertrophy