Preferred Name |
Klippel-Trenaunay syndrome |
|
Synonyms |
|
|
Definitions |
OMIM mapping confirmed by DO. [SN]. A syndrome that is characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues. |
|
ID |
http://purl.obolibrary.org/obo/DOID_2926 |
|
comment |
OMIM mapping confirmed by DO. [SN]. |
|
definition |
A syndrome that is characterized by large cutaneous hemangiomata with hypertrophy of the related bones and soft tissues. |
|
hasDbXref |
SNOMEDCT_US_2016_03_01:59078009 ICD10CM:Q87.2 UMLS_CUI:C0022739 OMIM:149000 MESH:D007715 NCI:C84801 |
|
hasExactSynonym |
angioosteohypertrophy syndrome Klippel-Trenaunay-Weber syndrome Haemangiectatic hypertrophy |
|
hasOBONamespace |
disease_ontology |
|
id |
DOID:2926 |
|
imported from | ||
inSubset | ||
label |
Klippel-Trenaunay syndrome |
|
prefixIRI |
DOID:2926 |
|
prefLabel |
Klippel-Trenaunay syndrome |
|
subClassOf |
This ontology integrates with OntoloBridge, allowing community users to suggest additions to the public ontology. Complete the template below to submit a term request directly to the ontology maintainer.
Term Label (required)
Suggested term name. If a term can be described with multiple synonyms, only list the preferred name here.
Term description (required)
A brief definition, description, or usage of your suggested term. Additional term synonyms may be listed in this section.
Superclass (required)
The parent term of the suggested term. The parent term should be an existing entry of the current ontology. The superclass can be selected directly from Bioportal's Classes tree viewer.
References (optional)
Provide evidence for the existence of the requested term such as Pubmed IDs of papers or links to other resources that describe the term.
Justification (optional)
Provide any additional information about the requested term here.