Allan-Herndon-Dudley syndrome
congenital disorder of nervous system
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Summary
Allan-Herndon-Dudley syndrome is a rare disease[1]. It draws 421 Wikipedia views per month (rare disease category, ranking #210 of 627).[2]
Key Facts
- Instance of: class of disease[3]
- Subclass of: complex hereditary spastic paraplegia[4], nervous system heredodegenerative disease[5], pure or complex X-linked spastic paraplegia[6], syndromic hypothyroidism[7], X-linked intellectual disability[8], peripheral hypothyroidism[9], X-linked recessive disease[10]
- NCI Thesaurus ID: C118843[11]
- Health specialty: medical genetics[12], neurology[13], pediatrics[14]
- Genetic association: SLC16A2[15]
- Exact match: http://purl.obolibrary.org/obo/DOID_0050631[16], http://identifiers.org/doid/DOID:0050631[17], http://www.orpha.net/ORDO/Orphanet_280270[18], http://www.orpha.net/ORDO/Orphanet_59[19]
- On focus list of Wikimedia project: WikiProject Medicine[20]
Why It Matters
Allan-Herndon-Dudley syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[21] It is known by 28 alternative names across languages and contexts.[22]