Klippel-Trenaunay-Weber Syndrome

Preferred Label : Klippel-Trenaunay-Weber Syndrome;

NCIt definition : A rare syndrome characterized by the presence of port-wine stain (a vascular malformation), varicose veins, and hypertrophy of the soft tissues and bones in an extremity. It usually affects one extremity, most commonly a leg.;

Details

Origin ID

C84801;

UMLS CUI

C0022739;

Currated CISMeF NLP mapping
- Angio-osteohypertrophic syndrome [ICD-11 Sub-sub category]
- Angio-osteohypertrophic syndrome (disorder) [SNOMED CT concept]
- Angioosteohypertrophic syndrome [ORDO Disease]
- Capillary-lymphatic-venous malformation with segmental distribution [ORDO Disease]
- Klippel Trenaunay Weber syndrome [Disease (Nov.)]
- Klippel-Trenaunay syndrome [DO Concept]
- Klippel-Trenaunay syndrome [MedDRA Preferred Term]
- Klippel-Trenaunay-Weber syndrome [MeSH Descriptor]
- Klippel-Trenaunay-Weber syndrome [MeSH concept]
- Klippel-Trenaunay-Weber syndrome [MedDRA LLT]
- Klippel-Trenaunay-Weber syndrome (disorder) [Inactive SNOMED CT concept]
- Klippel-Trénaunay syndrome [ICD-11 More detail]
- Klippel-trenaunay-weber syndrome [OMIM Phenotype]
- Parkes weber syndrome [OMIM Phenotype]
- klippel-trenaunay-weber syndrome [SNOMED Notion]
- weber klippel trenaunay [MeSH concept]
- weber klippel trenaunay [MeSH Supplementary Concept]
DO Cross reference
- Klippel-Trenaunay syndrome [DO Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Angio-osteohypertrophic syndrome (disorder) [SNOMED CT concept]
- Capillary-lymphatic-venous malformation with segmental distribution [ORDO Disease]
- Klippel Trenaunay Weber syndrome [Disease (Nov.)]
- Klippel Trenaunay syndrome (disorder) [SNOMED CT concept]
- Klippel-Trenaunay syndrome [DO Concept]
- Klippel-Trenaunay syndrome [MedDRA Preferred Term]
- Klippel-Trenaunay-Weber syndrome [MedDRA LLT]
- Klippel-Trenaunay-Weber syndrome [MeSH concept]
- Klippel-Trenaunay-Weber syndrome [MeSH Descriptor]
- Klippel-Trenaunay-Weber syndrome (disorder) [Inactive SNOMED CT concept]
- Klippel-trenaunay-weber syndrome [OMIM Phenotype]
- klippel-trenaunay-weber syndrome [SNOMED Notion]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- NICHD Terminology [NCIt concept]
- Neonatal Research Network Terminology [NCIt concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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