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721105004: Klippel Trenaunay syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3323526017 Klippel Trenaunay syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3323527014 Klippel Trenaunay syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Klippel Trenaunay syndrome Is a Congenital anomaly of skeletal bone false Inferred relationship Existential restriction modifier
Klippel Trenaunay syndrome Is a Multiple malformation syndrome with early overgrowth false Inferred relationship Existential restriction modifier
Klippel Trenaunay syndrome Is a Port-wine stain of skin true Inferred relationship Existential restriction modifier
Klippel Trenaunay syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
Klippel Trenaunay syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Klippel Trenaunay syndrome Finding site Structure of capillary of skin false Inferred relationship Existential restriction modifier 3
Klippel Trenaunay syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Klippel Trenaunay syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Klippel Trenaunay syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 2
Klippel Trenaunay syndrome Is a Angio-osteohypertrophic syndrome true Inferred relationship Existential restriction modifier
Klippel Trenaunay syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Klippel Trenaunay syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Klippel Trenaunay syndrome Finding site Structure of capillary of skin true Inferred relationship Existential restriction modifier 1
Klippel Trenaunay syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Klippel Trenaunay syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Klippel Trenaunay syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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