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1285323003: omgekeerd Klippel-Trénaunay-syndroom (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-May 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5246547019 Inverse Klippel Trénaunay syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5246548012 Inverse Klippel Trénaunay syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
14404111000146114 omgekeerd Klippel-Trénaunay-syndroom nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14404121000146116 cutaan hemangioom met spier- of botatrofie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14404131000146119 omgekeerd Klippel-Trénaunay-syndroom (aandoening) nl Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
14404141000146110 invers syndroom van Klippel-Trénaunay nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
5246549016 A rare vascular anomaly with the association of capillary and venous malformations with hypotrophy or shortening of an affected limb due to alterations in bones, muscles, or subcutaneous tissues. In most cases, at least one of the findings is noted shortly after birth, while the other components become evident later in infancy. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Inverse Klippel Trénaunay syndrome (disorder) Is a Capillary-venous malformation true Inferred relationship Some
Inverse Klippel Trénaunay syndrome (disorder) Is a Multiple malformation syndrome with limb defect as major feature true Inferred relationship Some
Inverse Klippel Trénaunay syndrome (disorder) Is a Longitudinal deficiency of limb true Inferred relationship Some
Inverse Klippel Trénaunay syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Inverse Klippel Trénaunay syndrome (disorder) Finding site Entire limb true Inferred relationship Some 1
Inverse Klippel Trénaunay syndrome (disorder) Associated morphology Abnormal shortening true Inferred relationship Some 1
Inverse Klippel Trénaunay syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Inverse Klippel Trénaunay syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Inverse Klippel Trénaunay syndrome (disorder) Finding site Structure of capillary blood vessel true Inferred relationship Some 2
Inverse Klippel Trénaunay syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Inverse Klippel Trénaunay syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Inverse Klippel Trénaunay syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Inverse Klippel Trénaunay syndrome (disorder) Finding site Venous structure true Inferred relationship Some 3
Inverse Klippel Trénaunay syndrome (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Inverse Klippel Trénaunay syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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