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24216005: Congenital absence (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
40644015 Congenital absence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
753828014 Congenital absence (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
40644015 Congenital absence en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
40644015 Congenital absence en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
40648017 Congenital aplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
40649013 Agenesis en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
40649013 Agenesis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
753828014 Congenital absence (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
753828014 Congenital absence (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Congenital absence (morphologic abnormality) Is a Aplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence (morphologic abnormality) Is a anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence (morphologic abnormality) Is a Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Congenital absence (morphologic abnormality) Is a Absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Congenital absence of all bilateral toes Associated morphology False Congenital absence (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital absence of all bilateral toes Associated morphology False Congenital absence (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 2
Common atrium with common atrioventricular junction (disorder) Associated morphology False Congenital absence (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Common atrium with separate arterioventricular junctions (disorder) Associated morphology False Congenital absence (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked hypodontia (disorder) Associated morphology False Congenital absence (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
X-linked oligodontia (disorder) Associated morphology False Congenital absence (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital complete absence of nasolacrimal drainage system (disorder) Associated morphology True Congenital absence (morphologic abnormality) Inferred relationship Existential restriction modifier (core metadata concept) 1

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