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66091009: 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
500308011 Congenital disorder en Synonym (core metadata concept) Active Entire term 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
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)


9391 descendants. Search Descendants:

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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