Hurler syndrome
genetic disorder that results in the buildup of glycosaminoglycans (AKA GAGs, or mucopolysaccharides) due to a deficiency of alpha-L iduronidase
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Hurler syndrome
Summary
Hurler syndrome is a malformation syndrome[1]. It draws 113 Wikipedia views per month (malformation_syndrome category, ranking #2 of 8).[2]
Key Facts
- Hurler syndrome's instance of is recorded as malformation syndrome[3].
- Hurler syndrome's instance of is recorded as class of disease[4].
- Gertrud Hurler is named after Hurler syndrome[5].
- Hurler syndrome's subclass of is recorded as mucopolysaccharidosis I[6].
- Hurler syndrome's OMIM ID is recorded as 607014[7].
- Hurler syndrome's BNCF Thesaurus ID is recorded as 21915[8].
- Hurler syndrome's Encyclopædia Britannica Online ID is recorded as science/Hurler-syndrome[9].
- Hurler syndrome's Orphanet ID is recorded as 93473[10].
- Hurler syndrome's NCI Thesaurus ID is recorded as C61261[11].
- Hurler syndrome's JSTOR topic ID is recorded as mucopolysaccharidosis-i[12].
- Hurler syndrome's GARD rare disease ID is recorded as 12559[13].
- Hurler syndrome's Microsoft Academic ID is recorded as 2777636572[14].
- Hurler syndrome's OpenAlex ID is recorded as C2777636572[15].
- Hurler syndrome's OpenAlex ID is recorded as C2910727661[16].
- Hurler syndrome's WikiProjectMed ID is recorded as Hurler syndrome[17].
Why It Matters
Hurler syndrome draws 113 Wikipedia views per month (malformation_syndrome category, ranking #2 of 8).[2] It has Wikipedia articles in 10 language editions, a strong signal of global cultural recognition.[18] It is known by 10 alternative names across languages and contexts.[19]