Peutz-Jeghers syndrome
autosomal dominant genetic disorder characterized by the development of benign hamartomatous polyps in the gastrointestinal tract and hyperpigmented macules on the lips and oral mucosa (melanosis)
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Peutz-Jeghers syndrome
Summary
Peutz-Jeghers syndrome is a rare disease[1]. It draws 458 Wikipedia views per month (rare_disease category, ranking #121 of 627).[2]
Key Facts
- Peutz-Jeghers syndrome's instance of is recorded as rare disease[3].
- Peutz-Jeghers syndrome's instance of is recorded as class of disease[4].
- Peutz-Jeghers syndrome is a type of intestinal disease[5].
- Peutz-Jeghers syndrome is a type of intestinal polyposis[6].
- Peutz-Jeghers syndrome's Commons category is recorded as Peutz–Jeghers syndrome[7].
- Peutz-Jeghers syndrome's ICPC 2 ID is recorded as A90[8].
- Peutz-Jeghers syndrome's NCI Thesaurus ID is recorded as C3324[9].
- Peutz-Jeghers syndrome's NCI Thesaurus ID is recorded as C4733[10].
- Peutz-Jeghers syndrome's NCI Thesaurus ID is recorded as C7755[11].
- Peutz-Jeghers syndrome's health specialty is recorded as medical genetics[12].
- Peutz-Jeghers syndrome's genetic association is recorded as STK11[13].
- Peutz-Jeghers syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3852[14].
- Peutz-Jeghers syndrome's exact match is recorded as http://identifiers.org/doid/DOID:3852[15].
- Peutz-Jeghers syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Peutz-Jeghers syndrome draws 458 Wikipedia views per month (rare_disease category, ranking #121 of 627).[2] It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[17] It is known by 22 alternative names across languages and contexts.[18]