Klippel–Trénaunay–Weber syndrome
syndrome that is characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues
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Klippel–Trénaunay–Weber syndrome
Summary
Klippel–Trénaunay–Weber syndrome is a designated intractable/rare disease[1]. It draws 139 Wikipedia views per month (designated_intractable_rare_disease category, ranking #101 of 201).[2]
Key Facts
- Klippel–Trénaunay–Weber syndrome's instance of is recorded as designated intractable/rare disease[3].
- Klippel–Trénaunay–Weber syndrome's instance of is recorded as class of disease[4].
- Maurice Klippel is named after Klippel–Trénaunay–Weber syndrome[5].
- Frederick Parkes Weber is named after Klippel–Trénaunay–Weber syndrome[6].
- Klippel–Trénaunay–Weber syndrome's subclass of is recorded as overgrowth syndrome[7].
- Klippel–Trénaunay–Weber syndrome's subclass of is recorded as syndrome[8].
- Klippel–Trénaunay–Weber syndrome's subclass of is recorded as PIK3CA-related overgrowth spectrum[9].
- Klippel–Trénaunay–Weber syndrome's subclass of is recorded as disease[10].
- Klippel–Trénaunay–Weber syndrome's Commons category is recorded as Klippel–Trénaunay syndrome[11].
- Klippel–Trénaunay–Weber syndrome's MeSH descriptor ID is recorded as D007715[12].
- Klippel–Trénaunay–Weber syndrome's OMIM ID is recorded as 149000[13].
- Klippel–Trénaunay–Weber syndrome's DiseasesDB is recorded as 29324[14].
- Klippel–Trénaunay–Weber syndrome's MedlinePlus ID is recorded as 000150[15].
- Klippel–Trénaunay–Weber syndrome's KEGG ID is recorded as H01788[16].
- Klippel–Trénaunay–Weber syndrome's GeneReviews ID is recorded as NBK52764[17].
- Klippel–Trénaunay–Weber syndrome's MeSH tree code is recorded as C14.907.077.410[18].
- Klippel–Trénaunay–Weber syndrome's eMedicine ID is recorded as 1084257[19].
- Klippel–Trénaunay–Weber syndrome's Disease Ontology ID is recorded as DOID:2926[20].
- Klippel–Trénaunay–Weber syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4600[21].
- Klippel–Trénaunay–Weber syndrome's Orphanet ID is recorded as 2346[22].
- Klippel–Trénaunay–Weber syndrome's Orphanet ID is recorded as 90308[23].
- Klippel–Trénaunay–Weber syndrome's NCI Thesaurus ID is recorded as C84801[24].
- Klippel–Trénaunay–Weber syndrome's different from is recorded as Parkes Weber syndrome[25].
- Klippel–Trénaunay–Weber syndrome's health specialty is recorded as medical genetics[26].
- Klippel–Trénaunay–Weber syndrome's BabelNet ID is recorded as 14792046n[27].
Why It Matters
Klippel–Trénaunay–Weber syndrome draws 139 Wikipedia views per month (designated_intractable_rare_disease category, ranking #101 of 201).[2] It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[28] It is known by 30 alternative names across languages and contexts.[29]