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402808004: Congenital vascular malformation due to inherited syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1770732017 Congenital vascular malformation due to inherited syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1781900011 Congenital vascular malformation due to inherited syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1770732017 Congenital vascular malformation due to inherited syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1770732017 Congenital vascular malformation due to inherited syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1781900011 Congenital vascular malformation due to inherited syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1781900011 Congenital vascular malformation due to inherited syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5864211000241117 anomalie congénitale vasculaire due à un syndrome héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5864221000241112 malformation d'un vaisseau sanguin due à un syndrome héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5864211000241117 anomalie congénitale vasculaire due à un syndrome héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5864221000241112 malformation d'un vaisseau sanguin due à un syndrome héréditaire fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital vascular malformation due to inherited syndrome (disorder) Is a Cutaneous vascular malformation (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital vascular malformation due to inherited syndrome (disorder) Finding site Blood vessel structure of skin (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital vascular malformation due to inherited syndrome (disorder) Associated morphology Congenital vascular anomaly false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital vascular malformation due to inherited syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital vascular malformation due to inherited syndrome (disorder) Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital vascular malformation due to inherited syndrome (disorder) Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital vascular malformation due to inherited syndrome (disorder) Finding site Blood vessel structure of skin (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital vascular malformation due to inherited syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital vascular malformation due to inherited syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital vascular malformation due to inherited syndrome (disorder) Finding site Blood vessel structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital vascular malformation due to inherited syndrome (disorder) Is a Congenital vascular malformation (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital vascular malformation due to inherited syndrome (disorder) Due to Hereditary disease true Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital vascular malformation due to inherited syndrome (disorder) Finding site Blood vessel structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital vascular malformation due to inherited syndrome (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital vascular malformation due to inherited syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital vascular malformation due to inherited syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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