About: Klippel-Trenaunay-Weber Syndrome

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Attributes	Values
rdf:type	Class
rdfs:label	Klippel-Trenaunay-Weber Syndrome
rdfs:subClassOf	Syndrome Rare Non-Neoplastic Disorder
Has_NICHD_Parent	Genetic Disorder
Concept_In_Subset	NICHD Terminology Neonatal Research Network Terminology
Semantic_Type	Disease or Syndrome
Preferred_Name	Klippel-Trenaunay-Weber Syndrome
UMLS_CUI	C0022739
Contributing_Source	NICHD
FULL_SYN	Klippel-Trenaunay-Weber SyndromePTNCI Klippel-Trenaunay-Weber SyndromePTNICHD
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.NCI
code	C84801

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