66091009: Congenital disease (disorder)

SNOMED CT Concept\constatation clinique\Disease\Congenital disease

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

10211000188115 pathologie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

109766011 Congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

3921000077116 maladie congénitale fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

660561000077119 maladie congénitale (trouble) fr Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Common French translation module (core metadata concept)

805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital disease	est un(e) (attribut)	Disease	true	Inferred relationship	Some
Congenital disease	survenue (attribut)	congénital	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary factor IX deficiency disease (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Hereditary factor XI deficiency disease (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
Congenital forefoot varus	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital rearfoot varus	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital malformation	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
anomalie morphologique congénitale	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
reliquat embryonnaire	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Congenital melanosis (disorder)	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some
structure dysmorphique	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Cor biloculare	est un(e) (attribut)	False	Congenital disease	Inferred relationship	Some
Chuvash erythrocytosis	est un(e) (attribut)	True	Congenital disease	Inferred relationship	Some

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This concept is not in any reference sets