Cowden syndrome 1
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Summary
Cowden syndrome 1 is a class of disease[1]. It draws 1,621 Wikipedia views per month (class of disease category, ranking #518 of 1,968).[2]
Key Facts
- Subclass of: autosomal dominant disease[3], multiple hamartoma syndrome[4], syndrome[5]
- Commons category: Cowden syndrome[6]
- NCI Thesaurus ID: C3076[7]
- Health specialty: oncology[8], medical genetics[9], gastroenterology[10], neurology[11]
- Genetic association: PTEN[12]
- Exact match: http://purl.obolibrary.org/obo/DOID_6457[13], http://identifiers.org/doid/DOID:6457[14], http://www.orpha.net/ORDO/Orphanet_201[15]
- On focus list of Wikimedia project: WikiProject Medicine[16]
Why It Matters
Cowden syndrome 1 has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[17] It is known by 28 alternative names across languages and contexts.[18]