66091009: Congenital disease (disorder)

SNOMED CT Concept\Clinical finding (finding)\Disease\Congenital disease (disorder)

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

109766011 Congenital disease en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
109767019 Congenital disease, NOS en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
500309015 Congenital abnormality en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
500310013 Fetal developmental abnormality en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
805666017 Congenital disease (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3011638011 Foetal developmental abnormality en Synonym (core metadata concept) Inactive Only initial character case insensitive (core metadata concept) SNOMED CT core
2478441000052112 medfödd sjukdom sv Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Sweden NRC maintained module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Congenital disease (disorder)	Is a	Disease	true	Inferred relationship	Some
Congenital disease (disorder)	Occurrence	Congenital	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
X-linked corneal dermoid (disorder)	Is a	True	Congenital disease (disorder)	Inferred relationship	Some
X-linked neurodegenerative syndrome Bertini type (disorder)	Is a	True	Congenital disease (disorder)	Inferred relationship	Some
Isolated generalized anhidrosis with normal sweat glands	Is a	True	Congenital disease (disorder)	Inferred relationship	Some
Non-syndromic mitochondrial sensorineural deafness (disorder)	Is a	True	Congenital disease (disorder)	Inferred relationship	Some
Neuropsychiatric disorder	Is a	True	Congenital disease (disorder)	Inferred relationship	Some

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This concept is not in any reference sets