Cowden syndrome 1
inherited disorder causing tumor-like growth and increased cancer risk
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Cowden syndrome 1
Summary
Cowden syndrome 1 is a class of disease[1]. It draws 341 Wikipedia views per month (class_of_disease category, ranking #518 of 1,968).[2]
Key Facts
- Cowden syndrome 1's instance of is recorded as class of disease[3].
- Cowden syndrome 1 is a type of autosomal dominant disease[4].
- Cowden syndrome 1 is a type of multiple hamartoma syndrome[5].
- Cowden syndrome 1 is a type of syndrome[6].
- Cowden syndrome 1 is a type of disease[7].
- Cowden syndrome 1's Commons category is recorded as Cowden syndrome[8].
- Cowden syndrome 1's NCI Thesaurus ID is recorded as C3076[9].
- Cowden syndrome 1's health specialty is recorded as oncology[10].
- Cowden syndrome 1's health specialty is recorded as medical genetics[11].
- Cowden syndrome 1's health specialty is recorded as gastroenterology[12].
- Cowden syndrome 1's health specialty is recorded as neurology[13].
- Cowden syndrome 1's genetic association is recorded as PTEN[14].
- Cowden syndrome 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_6457[15].
- Cowden syndrome 1's exact match is recorded as http://identifiers.org/doid/DOID:6457[16].
- Cowden syndrome 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_201[17].
- Cowden syndrome 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
Cowden syndrome 1 draws 341 Wikipedia views per month (class_of_disease category, ranking #518 of 1,968).[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[19] It is known by 17 alternative names across languages and contexts.[20]